PROSPECTUS - igmpiindia · PROSPECTUS DRUG DISCOVERY AND DEVELOPMENT PHARMACEUTICAL CHEMISTRY ......

PROSPECTUS

DRUG DISCOVERY AND DEVELOPMENT

PHARMACEUTICAL CHEMISTRY

BIOINFORMATICS

PHARMACEUTICAL FORMULATION AND ENTREPRENEURSHIP

HERBAL DRUG TECHNOLOGY

PHARMACEUTICAL PROCESS ENGINEERING

PHARMACEUTICAL TECHNOLOGY TRANSFER

Distance cum e-learning modes

Faculty of Drug Discovery and Development

[ FDDD ]

POST GRADUATE /EXECUTIVE DIPLOMA IN:

IGMPIInstitute of Good Manufacturing Practices IndiaGlobal accredited training & certification providerConferred with QUALITY COUNCIL OF INDIA (QCI) – D.L. SHAH NATIONAL QUALITY AWARD &ASSOCHAM Services Excellence Award 2017

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A well learned person is most respected individual. If professional growth is deserved in today's competitive world, knowledge, training and professional skills are important!

Founder's views on Drug Discovery and Development programmes:Drug development is an important aspect of human healthcare today. The industry is changing face rapidly with new tools, technologies and changing needs of the target audience. Thus their exists an increasing need for a group of learned and scientifically trained professionals who are well versed with the drug discovery needs, importance, tools, global scenarios and rational aspects as well. Founder and multidisciplinary faculty at IGMPI has tapped this upcoming boom in the Drug Discovery and Development sector by laying format for the well-structured Diploma courses to serve the need. IGMPI's distance cum e-learning courses in Drug Discovery and Development framed to make our candidates up and available to get hold onto best employment options in this industry.

Founders' Views on Pharmaceutical Chemistry Programmes:The field of Pharmaceutical chemistry is quite diverse, challenging and has a very broad scope. Drug discovery, development as well as characterization is an important aspect of human healthcare today. The industry is changing face rapidly with new tools, technologies and changing needs of the target audience. Thus their exists an increasing need for a group of learned and scientifically trained professionals who are well versed with the drug discovery needs, importance, tools, global scenarios and rational aspects as well.

Founder and multidisciplinary faculty at IGMPI has tapped this upcoming boom in the Pharmaceutical Chemistry sector by laying format for the well-structured Diploma courses to serve the need.

IGMPI's distance cum e-learning courses in Pharmaceutical Chemistry have been framed to make our candidates up and available to get hold onto best employment options in this industry.

Founders' Views on Bioinformatics ProgrammesBioinformatics is the most rapidly developing field of modern scientific endeavor. In last 20 years alone major developments in techniques have led to significant biological and medical breakthroughs, encompassing a systematic development and application of IT solution to handle biological information or data obtained by experiments, modeling, database, search and instrumentation. It touches all areas of biology, with application to genome analysis, protein structure, prediction, target identification, drug-design, and metabolomics and systems biology.

IGMPIs Post Graduate and executive diploma programme offers an opportunity to spread enhance and share knowledge in the emerging areas of Bioinformatics. To provide quality inputs in the area of Bioinformatics, to working professionals and individuals who have completed their education and willing to contribute in this area.

Benefits of Bioinformatics

Bioinformatics has become an important part of many areas of biology.

In experimental molecular biology, bioinformatics techniques such as image and signal processing allow extraction of useful results from large amounts of raw data.

In the field of genetics and genomics, it aids in sequencing and annotating genomes and theirobserved mutations.

It plays a role in the text mining of biological literature and the development of biological andgeneontologies to organize and query biological data.

It also plays a role in the analysis of gene and protein expression and regulation.

Founder’s View on Pharmaceutical Formulation and EntrepreneurshipThis course will endow professionals with the skills and knowledge to allow them to join effectively in the conception and growth of high impact pharmaceutical business ventures. The professionals will be idyllically positioned to commence their own startup companies and unite with existing pharmaceutical business. Students will learn how to widen and evaluate a new business notion and how to hoist finance for and market a business and its output. This programme is inimitable in equipping students with a wide-ranging skill set in both medicines design entrepreneurship. The professional will also gain complete knowledge of formulation development and gain familiarity with the tasks performed in formulation and development space.

Founders View on Herbal Drug TechnologyHerbal medicine is undoubtedly the oldest system of medical science in the world. Utilization of nature's wealth for health benefits and the cure, prevention and mitigation of diseases plays a big role in human civilization, with a dependency of a large number of human populations particularly in developing countries.With the advancement of modern technology, people have paved up to a new era of herbal medicine. Advanced technologies have boosted the growth of herbal industry and created immense global interest towards herbal medicine. The advancement in the technologies have also helped the developed countries to adopt this ancient and enriched medicinal system in a new way. Public demand has also grown for evidence on the safety, efficacy and quality of herbal products. Founder and multidisciplinary faculty at IGMPI has tapped this upcoming boom in the Herbal Drug Technology sector by laying format for the well-structured Diploma courses to serve the need.

Founder View on Pharmaceutical Process EngineeringThe founders of IGMPI understand the need of Pharmaceutical Process Engineering programme to empower the participants to develop and expand their technical and management knowledge keeping in mind the immense scope of engineering application in today's rising era of pharmaceutical industries worldwide. Thus, the vision of offering reliable and up-to-date information in the form of appropriate course and training programmes designed by known members and experts of the industry has been given shape by IGMPI. The course also teaches the dissemination and engineering which involves in translating the needs of the customer into production facilities that convert "raw materials" into value-added components. Process engineering is the branch of engineering that is concerned with industrial processes i.e. batch and continuous processes such as the production of drugs, solvents, Refrigerants, pesticides etc

Process Engineers as a part of pharmaceutical EngineeringSummarizing fundamental engineering principles and operations critical to converting bulk pharmaceutical products into patient-ready and appropriate drug delivery dosage forms, Pharmaceutical Process Engineering facilitates comprehensive understanding of the practical aspects of drug production in an accessible, step-by-step format. It provides a pharmaceutical perspective on unit operations that improves communication among diverse professionals in the field-from pharmaceutical researchers to chemical and industrial engineers-and fully covers the relationship of pharmaceutical development to the application of key concepts and major unit operations in pharmaceutical engineering.

Founder's View on Pharmaceutical Technology Transfer'Make in India' programme demands highly skilled and technically sound personnel's to further the prospects of commercialization and technology transfer from research labs to manufacturing units. Certainly companies need to be market competitive and to achieve this there is a growing demand of certified professionals. Technology transfer (TT) includes knowledge transfer, science and risk-based principles including ICH Q8, Q9, Q10, Q11 and efficient processes to meet evolving business needs. Appropriate technology transfer is both integral and critical to drug discovery and development for new medicinal products. It is also important to upgrade drug quality designed during research and development and to finalize product during manufacturing as well as to assure stable quality. This course will provide a thorough understanding of the technology transfer of analytical methods, quality control standards, packaging components, operations and various pharmaceutical dosage forms from R&D to manufacturing. It is designed to provide an understanding of the issues affecting the transfer within and outside a company.

Objectives of Pharmaceutical Technology Transfer programmesBy the end of this course, it is intended that students who have successfully completed all the course requirements will be able to:

Demonstrate specialized knowledge of technology transfer and commercialization techniques.

Demonstrate mastery of theoretical knowledge of technology transfer and technology

Identification methods and practice to generate solutions for development and commercialization plans.

Investigate, critically reflect on and effectively communicate in plain English to inform diverse audiences of complex theoretical and practical ideas, concepts, strategies and courses of action concerning technology transfer.

Demonstrate relative cognitive and creative skills to analyze and synthesize complex information and problems at a theoretical level to then develop, justify and apply solutions at a practical level particularly to advice on transactions or interactions involving technology transfer.

Demonstrate learning of intellectual property rights and reflect upon understanding of patents documents and patentability requirements. The incumbent should be able to understand the complete patenting process

Autonomously design, theorize, plan, execute and evaluate a substantial research-based project on a technology transfer and commercialization topic

Learning and re-learning are important steps to success!Keeping in mind, all needs and requirements of the industry; founders of IGMPI and leaders and important contributors from the drug discovery industry have brought to light a distance cum e-learning course to cater all needs of this industry and its aspirants.

With this course, the aspirants will be appropriately equipped to face any and every challenge the industry throws to them. The course offers:

Subject learning,

Work knowledge of each face of the industry,

Case study based approach ensures on-field problem handing;

Training in professional etiquettes, ethics and varied working tools of the industry;

Drug Discovery and Development, PharmaceuticalChemistry, Bioinformatics and Pharmaceutical Formulation and Entrepreneurship Courses by IGMPIThe academic training in drug development forms the base but they need to be backed with professionals training. Diploma courses by IGMPI add to the candidate's potential of entering into this industry by offering:

Complete knowledge of the theoretical chapters (structural design, rational and combinatorial methods, drug target selection etc.)

Knowledge and training of practical drug designing tools

Application and technicalities of drug development process

Guidance by field experts during the course and drug patenting

Knowledge of global scenarios, scope and opportunities

Knowledge about the clinical trials, ethics and regulatory processes involved.

IGMPI course promise to polish the skills of its candidates and make them job ready! The candidates are taught the techniques, given practical knowledge and accustomed to the varied on-field situation that might arise during their careers. All this is made possible with help of extensive course material which has been designed by experts who are or have been contributing to the industry in the past; The existing professionals also have lots to learn and explore through these course.

Drug Discovery and Development- An important and booming field in the Healthcare Industry!Healthcare is a huge world today with varied faces and aspects. Drug Discovery and Development is one such important and booming field. This sector of healthcare industry is meant for research enthusiasts. Proper blend of knowledge and professionalism is needed here. All this is complimented

by the respect, credibility and financial security for its takers. IGMPI has added a feather to its existing bouquet of distance cum e-learning courses with an extensive Post Graduate Diploma and Executive Diploma Courses in Drug Discovery and Development. The sector is gaining importance because of the increasing need of better treatment methods and drugs and thus drug discovery is an upcoming field of work. The expertise required excelling in the field of drug discovery and development is multi-faceted. An individual with all round information about the varied theoretical and practical aspects of this field can only do well and successfully sustain through the work life in this industry type. At IGMPI, efforts have been made to design and structure a well-knit course which covers all aspects of the industry; be it history of drug development, drug designing tools, latest drug development models, drug approval process (in Indian and International market), reviewing drug designs, targeted drug development or any other parameter related to this industry. The course moulds book knowledge but offers guidance by professionals from the industry to make sure the candidates are well groomed to handle different scenarios and come out as well trained and efficient employees of the industry. Serving drug development and design industry is a hard task as it needs knowledge about the practical tools, latest technologies and future of these tools as well. The candidate need to have insight of the current practices of the industry plus should have apt information and opinion about the direction the industry is heading in and future of the same. With all this information and training, IGMPI candidates would present to be effectively productive and well groomed to complement personnel needs of the industry as well.

Pharmaceutical Chemistry: An integral component of the Drug Industry Pharmaceutical Chemistry is the backbone of the Pharmaceutical Industry as it deals with the

process of identification, discovery, synthesis and formulation of new active chemical compounds. Pharmaceutical chemists use their research skills to formulate, produce, characterize, and analyze new compounds for specific applications. The field offers immense opportunities in pharmaceutical industries and labs. Typical careers of pharmaceutical chemistry graduates include assistant analyst, development chemist, research assistant, and site chemist. The main employers of chemistry graduates are in the chemical and related industries, such as:

pharmaceuticals;

plastics and polymers;

agrochemicals;

metallurgical;

petrochemicals;

toiletries.

However, they may also find opportunities with employers in many different sectors, including the food and drink industry, utilities and research, health and medical organisations, government, and scientific research organisations and agencies. Pharmachemistry post-graduates are also employed in schools, colleges and universities, as well as by computer software development companies, environment consultancies and water companies.

Bioinformatics: Science of the millenniumAn unparalleled affluence of biological data has been generated by the human genome project and sequencing projects in other organisms. The huge demand for analysis and elucidation of these data is

being managed by the evolving science of bioinformatics. Bioinformatics is defined as the application of tools of computation and analysis to the capture and interpretation of biological data. It is an interdisciplinary field, which harnesses computer science, mathematics, physics, and biology. Bioinformatics is essential for management of data in modern biology and medicine.

Pharmaceutical Formulation and Entrepreneurship: Frontage in new product developmentFormulation development is a key area of product development that can verify patentability, lifecycle and, eventually, the success of a pharmaceutical product. Pharmaceutical companies integrate formulation development functions and personnel into their product development cycle in many different ways. In fully incorporated large pharmaceutical companies, definite departments may exist to deal with such areas as the physical characterization of drug substances and formulation issues. In many cases, other departments, often in other buildings or locations, may handle preclinical functions, such as animal testing. These departments must work closely to gain a complete understanding of their unique drug substance.

Herbal Drug Technology: Technology Attributing ResurgenceHerbal medicine has been commonly used over the years for treatment and prevention of diseases and health promotion as well as for enhancement of the span and quality of life. Treatment of illness and maintenance of health using herbal medicines is the oldest and most popular form of Healthcare practice known to humanity that has been practiced by all cultures in all ages throughout the history of civilization. An improvement in each step of herbal medicine production has recently been possible with the aid of technical developments. The increase in the demand and utilization of herbal medicine in the past few years has been increased considerably indicating herbal 'renaissance'. The current trend of utilization of these formulas after scientific researches and modern technological aspects helped in industrial growth of herbal medicine. Governments, international agencies and corporations are increasingly investing in traditional herbal medicine research.

A Distance cum E-learning course provides better and easy access to required knowledge.IGMPI offers professional and industry oriented training thus opening doors for entry into the industry. Diploma Courses in Pharmaceutical Chemistry as well as Drug Discovery and Development are designed to be an advantage for those already in the industry as a tag of professional training and those new to the industry feel comfortable with backing of apt and up-to-date information and training required to have sustained growth in the industry. The web portal has been intelligently designed to end the hassles of finding a reliable but at the same time easily accessible information provider. The course and training programs cater needs of the varying categories of prospective candidates. All candidates can apply for course and pursue the same at their own pace, with success being determined at end of each course as well as training program through set of periodic assignments and online exams. With the courses in Drug Discovery and Development, IGMPI crosses another yard stick and moves ahead towards its goal of offering quality professional education in a format easy to understand and follow for prospective candidates. Its strategy of making reliable

information easily accessible stays satisfied through this new course and IGMPI here again promises to polish skills and groom its candidates to compliment industry needs and be assets for the drug discovery industry by making apt use of their training and knowledge.uter software development companies, environment consultancies and water companies.

IGMPI: A yard stick crossed and many more to go! In all, IGMPI targets to fill up the gap between the existing and accessible knowledge about varied aspects of Public Health and Hospital Management Industry from strategies to analysing scenarios, to operations, making new strategies, executing current programmes and everything else. Through the user friendly, well designed and appropriately featured web site, founders of IGMPI offer to join hands with the existing employees and those targeting to be a part of this industry type. Thus, offering to provide all knowledge and information you might need about basics, history, formulation and application strategy, compliance, marketing rules, significance in import and export of goods, regulatory authorities, application methods, anticipating problems and fixing quality issue.

About IGMPIInstitute of Good Manufacturing Practices India, registered as a non-profit society ( under The Societies Registration Act,1860) with Government of India recognised by the Department of Industrial Policy & Promotion, Ministry of Commerce & Industry, Government of India, accredited Vocational Institution of Ministry of HRD, Government of India, approved training Institute of Food Safety and Standards Authority of India (FSSAI) and affiliated with Life Sciences Sector Skills Council (SSC) and Food Industry Sector Skills Council of National Skill Development Corporation (NSDC) -presents unique, friendly and interactive platform to get rid of all your GMP related glitches. GMP- is an essential element of industries like pharmaceutical, cosmetic, Ayurveda, biotech, homeopathic, medical device and food manufacturing. GMP in itself is the most dynamic part which witnesses frequent changes in terms of newer rules being added and older ones being renewed. Keeping self updated with current GMPs thus becomes inevitable to stay abreast with the changing industry needs and practices.

Our group of learned professionals from above mentioned sectors of the Pharma, Healthcare and Food industries have put together their knowledge; know about and practical experiences in form of this GMP guide. IGMPI is moving hand in hand with technology advances and has gained recognition as stronger and better training platform provider for professionals and students in the aeas of GMP, Quality Assurance and Control, Pharma, Food and healthcare Regulatory Affairs, Clinical Research, Pharmaceutical IPR and Good Laboratory Practice and Product Management. The importance of quality healthcare and foods is known to our founders and thus numerous efforts are being made to offer friendly but effective and easy regular, part-time and online/distance sources of GMP training, Quality Assurance and Control, Pharma and healthcare Regulatory Affairs, Clinical Research, Pharmaceutical IPR and Good Laboratory Practice in form of formal classroom studies, distance/online/interactive courses, online seminars, as well as onsite training programmes along with knowledge of worldwide affairs of the industry; in short a round-the-clock help for any information in these areas needed by anybody from around the world. Based on high standard of quality, the training programmes in Pharma, Healthcare and Food GMP, Quality Assurance and Quality Control, Regulatory Affairs, IPR, Pharma Product Management, Public Health, Hospital Management, Clinical Research, Pharmacovigilance, Medical Writing, Medical Coding, Nanotechnology, Drug Design and Discovery, Food QA&QC etc areas have been approved by Quality Council of India, which is an autonomous body and an accreditation authority for education & vocational training providers under the Department of Industrial Policy & Promotion, Ministry of Commerce & Industry, Government of India.

The IGMPI's team of technology experts and other Industry advisors together pursue to make cGMP knowledge, training in the area of Pharma and Food manufacturing easily accessible, through this platform.

About Faculty of Drug Discovery and Development (FDDD)The Faculty of Drug Discovery and Development (FDDD) is dedicated for providing education and training, news updates through newsletters covering national and international news and analysis on all aspects of drug discovery and development, recent research in chemistry, drug development and identification methods. FDDD is guided by brilliant, dynamic faculty members trained in various top CROs, SMOs and pharmaceutical industries possessing cutting edge technical expertise/skills and dedicated to teaching and research allowing new industry integrated programmes in pharmaceutical chemistry, drug discovery and development, drug analysis and identification and chemistry of medicines from natural sources. The FDDD team of technological experts has launched a high profile multi-tiered program to cater to the needs of knowledge intensive biotech /biopharma/ health care industry at different levels of employment, as well as that of academics. The FDDD team of technology experts and other Industry advisors together pursue to make knowledge in drug discovery and development, drug analysis and standardization drug development training in the area of Pharma and healthcare easily accessible, through this platform.

Accreditation and AwardsInstitute of Good Manufacturing Practices India (IGMPI) is registered as a non-profit society with its own Memorandum of Association and bye-laws under The Societies Registration Act, 1860, Government of India.

IGMPI is recognized by Department of Industrial Policy & Promotion, Ministry of Commerce & Industry, Government of India and is an accredited Vocational Institution of Ministry of HRD, Government of India (AVI no-710367) and all the courses of IGMPI are approved for life time empanelment under Ministry of Horticulture and Food Processing, Government of Uttar Pradesh also.

The quality based Post Graduate and Executive Diploma programmes of IGMPI in Good Manufacturing Practices, Regulatory Affairs, Intellectual Property Rights, Quality Assurance and Quality Control, Public Health, Nanotechnology, Product Management, Sales and Marketing Management, Clinical Research, Medical Writing, Drug Discovery and Development, Pharmacovigilance, Medical Coding have been duly assessed and approved by Quality Council of India, Government of India based on fulfillment of following criteria:

1. Course Content

2. Course Design

3. Course Material

4. Instructors

5. Class size & Attendance

6. Facilities

7. Evaluation of Students

8. Written Examination

9. Certificate

IGMPI is also an ISO 9001:2015 Certified Organisation accredited under Dubai Accreditation Center (DAC), Accreditation Department, Government of Dubai, UAE and has been conferred with QUALITY COUNCIL OF INDIA (QCI) – D.L. SHAH NATIONAL QUALITY AWARD – Certificate of Merit 2015 & ASSOCHAM Services Excellence Award 2017.

IGMPI is affiliated with Life Sciences Sector Skills Council (SSC) and Food Industry Sector Skills Council set up by National Skill Development Corporation (NSDC) as well.

IGMPI is an approved Training Institute of Food Safety and Standards Authority of India (FSSAI)(FSSAI ID: TPINS18) IGMPI PHARMA® is licensed by Department of Food Safety & Drug Administration under the Drugs and Cosmetics Act, 1940 and registered under Food Safety and Standards Act 2006.

IGMPI is a PMKVY (Pradhan Mantri Kaushal Vikas Yojna) affiliated training partner ( SMART TP Number: Tp010908)

IGMPI also offers International Register of Certificated Auditors (IRCA) Accredited Lead Auditor course periodically.

IGMPI is also registered under Section 23 (2), Rule 56 (1), Trade Marks Act, 1999, Government of India (Reference No. 2738626).

Quality Council of India (QCI)Quality Council of India is set up by the Government of India to establish and operate national accreditation structure and promote quality through National Quality Campaign. QCI is registered as a non-profit society with its own Memorandum of Association. QCI is governed by a Council of 38 members and Chairman of QCI is appointed by the Prime Minister on recommendation of the industry to the government. The Department of Industrial Policy & Promotion, Ministry of Commerce & Industry, is the nodal ministry for QCI.

National Accreditation Board for Certification Bodies (NABCB), Quality Council of India is a member of International Accreditation Forum (IAF) & Pacific Accreditation Cooperation (PAC) as well as signatory to its MLAs for Quality Management Systems, Environmental Management Systems and Product Certification. NABCB is also a Full Member of International Laboratory Accreditation Cooperation (ILAC) & Asia Pacific Laboratory Accreditation Cooperation (APLAC) as well as signatory to its MRAs for Inspection.

National Skill Development Corporation (NSDC)The National Skill Development Corporation (NSDC), working under the aegis of the Ministry of Skill Development and Entrepreneurship, is an apex organization for skill development in the country. The NSDC is responsible for overseeing the many Sector Skill Councils as well as other skill development and promotional activities across the country. It also implements many Government of India skill schemes such as Pradhan Mantri Kaushal Vikas Yojana (PMKVY) and UDAAN.

NSDC was set up by the Government of India as part of the national skill development mission in order to fulfill the growing need for skilled manpower across sectors. The Chairman of NSDC is nominated by Government of India.

ADVISORY BOARD AND TEAMDr. Mahesh C Gupta, Chief Advisor: Dr. Mahesh C Gupta is an experienced and internationally reputed Scientist in the field of calibration, quality assurance and testing. He has worked with many government organizations like National Physical Laboratory (NPLI), New Delhi for 32 years and later with Dubai Central Laboratory, Dubai as Principal Quality Officer. He has also played a vital role in developing lab accreditation program of India as Head National Calibration Program. He is also the founder president of Indian quality association. He has expertise and proficiency in various fields like calibration, GLP, analytical techniques, quality assurance, laboratory inter-comparison, proficiency testing, QMS and many more. With his knowledge and rich experience, he is focused on practical aspects of current needs, contemporary and emerging trends, besides alerting the laboratories for future challenges. A PhD from Indian Institute of Technology (IIT), New Delhi, Dr. Mahesh C Gupta has been associated as a research fellow of Optical Society of India, Fellow of Indian Society of Lighting Engineers and Vacuum society of India. He is also currently managing Lab World Magazine –a renowned world class magazine dedicated to Quality Testing and Calibration laboratories in all sectors- as the Editor in Chief.

Mr. Vinod Kumar Arora, Principal Advisor: Mr. Vinod Kumar Arora is an internationally acclaimedindustry professional having 35 years of rich experience in pharmaceutical development in the areas of Generics, Differentiated, NDDS/NCE Dosage Forms. He is now associated with IGMPI as an advisor.

He joined Ranbaxy in 1983 where he initially worked as scientist for almost 4 years. He rejoined Ranbaxy in 1994 where graduated to Vice President level from Assistant Director position. During his association with Ranbaxy he developed products - Generics, Differentiated Generics, NDA's and NCE-Global, market specific and OTC. Prior to his association with Ranbaxy, he worked as an Assistant General Manager with the Formulation Development Research in Cadila Laboratories, Ahmedabad and helped in setting up of Onco-manufacturing facility and developed several oncology products. He has expertise in Dosage Form development in the area of dosage forms – Solids -Tablets / Capsules / Granules / Pellets /PFOS/TFOS; Non-solids –Liquid /Injectables including Lyophilised/Topicals, Inhalations – DPI/ pMDI and Nasal Spray, Dosage Forms Technology such as Nanotechnology, Depot Injection; Modified Release tablets/suspension, Self-Emulsifying System, Oro dispersing tablets/oro -

dissolving strips; Particles/Pellets coating and has good understanding of current Good Manufacturing Practices and QA/QC. He has made presentations to NDAC Committee for New Drugs Approval in India, had meetings with Oman MOH and Pre IND meetings with USFDA. He has also authored/coauthored over 100 patents in the area of NCE/ Differentiated products /NDDS/Generics. With his knowledge and rich experience, he is focused on practical aspects of current needs, contemporary and emerging trends, besides alerting the pharmaceutical industries for future challenges. He is holding many honorary positions -Member of Indian Pharmacopoeia Scientific Body , Panel member of INMAS-DRDO, Ranbaxy Science Foundation Scholars Award , Global Expert committee member of DFE Pharma , Germany and Distinguished Scientist from World Whos Who Society , Member of Indian Pharma Committee of Make in India Campaign etc. He was felicitated by Hon'ble former President of India, Dr A P J Abdul Kalam for development and launch of first NCE – Anti malarial from India. Mr. Vinod Arora is a M. Pharm degree holder from BHU and DBM from IMM, New Delhi. As one of our principal advisors he will be supporting our initiatives nationally and internationally to rest of faculty members of IGMPI in imparting education, training and continuing education programs as well as our knowledge dissemination initiatives like Current GMP,QA/QC, Regulatory affairs ,Clinical research guidelines and news updates.

Mr. Syed Q. Abbas, Advisor: An eminent and a dynamic person, with a rich experience of 37 years in the food Industry. Prior to associating with IGMPI, Mr Abbas has been working in the Food Corporation of India under both state and central governments in the various departments. He has specialized experience in Storage and Preservation of food grains, Quality Assurance and Quality Control & Supply Chain Management. He has a rich exposure in food safety and quality. He has successfully carried out audits, faced CAG and statutory audits for food safety and quality in the FCI. He has provided trainings and has organized a series of workshops for food professionals. He is presently active in providing our Faculty of Food Safety & Quality his valuable leadership to take it to the new level in the future.

Ms. Rajni Jha, Advisor: Ms. Rajni Jha, an expert professional in International Regulatory Affairs and Quality Assurance for APIs for US, European as well as Asia-Pacific markets completed her M.Sc. and Post M.Sc Research work from I.I.T., Kanpur. She has more than 20 years of rich experience working with various pharmaceutical companies like Ranbaxy, Morepen Laboratories, Torrent Pharma, Nicholas Piramal, Unimark Labs, Glenmark Generics and Indswift Labs Ltd.

She is associated with IGMPI for development of training modules , e-lectures, personal lectures, workshops etc. Owing to her skills and proficiency; she had been leading a team of both RA and QA personnel from different departments. Her key responsibilities and roles included submission of API Dossiers including Drug Master Files (DMFs), Technical Data Packages (TDPs) and their updates, Supplements, Amendments, Responses to Queries of different Intermediates & APIs for Filing purposes to Regulatory authorities of various countries as per current global Regulatory guidelines for approvals across all markets (USA, Europe, Australia, Latin America, Asia Pacific, Russia, etc.), development and upgradation of various Protocols /Checklists for CQA as well as RA, assessment of various outsourced DMFs and maintenance of existing DMFs, preparation and streamlining of SOPs, etc. She has also successfully completed USFDA, PMDA, TGA, MHRA and Greece Authority audits for GMP compliance for outsourced intermediates and APIs as a part of QA function. She has attended various conferences/seminars on Regulatory Affairs, Quality Assurance and compliance through both domestic and International training programs. She has also been actively involved in imparting internal training and creating awareness on current GMP requirements, data generation with respect to regulatory requirements and updating of systems with current regulatory requirements across different departments in various organizations through training modules and workshops.

Dr. Manjusha Rajarshi, Advisor: Dr. Manjusha Rajarshi has more than 20 years of rich experience in the pharmaceutical industry (various companies -Bayer, Aventis Pasteur, Unichem, B. Braun); Her various career moves from training department, medical department, clinical operations and regulatory affairs and medical affairs. Her industry exposures include: Clinical trial sites and sponsor sites audited for GCP compliance; PV skills assessed via PV inspections of EMA from global headquarters; for 4 years, Local Person Responsible for PV, with Servier, India. She is honourable member of i) the Medical Committee with OPPI (organization of Pharmaceutical Producers of India), member of the committee for deliberations of GCP guidelines, PV guidelines to the Indian Regulatory Authorities ii) Pharmacy Council of India (PCI), iii) Indian Society of Clinical Research (ISCR), iv) Indian Association for Statistics in Clinical Trial. Besides, therapeutic areas handled by her are cardiology, diabetology, venous diseases, neuro-psychiatry, vaccines and many other internal medicinal therapies. She has more than 25 publications published on behalf of international journals such as IJCP, American Journal of Cardiovascular Drugs, Neurology, International Journal of Cardiology, Diabetes Research etc

Ms. Amrita Bhattacharya, Associate Professor: Amrita is associated with IGMPI as an Associate Professor. She is engaged in developing modules, e-lectures at her best in the disciplines of Good Manufacturing Practices, Clinical Research, Quality Assurance, Quality Control, Pharmacovigilance, Public Health & Hospital Administration. She has worked with many pharmaceutical & healthcare companies like many pharmaceutical companies like Fortis Clinical Research and Jubilant Clinsys having more than 6 years of experience. She has successfully conducted clinical studies for US FDA, EMEA, DCGI & for several reputed Pharma companies. She is also having technical expertise in conducting Clinical Trials Phase I & Phase II. Amrita has also performed pre-qualification and post-qualification audits for Quality Assurance & Quality Control & Good Manufacturing Practices. Amrita has completed her graduation in Microbiology from Lady Amritbai Daga &Smt. Ratnidevi Purohit College for Women, Nagpur and Master's Degree in Biotechnology from Rani Durgavati University, Jabalpur.

Ms. Sneha Gupta, Senior Faculty Member: She is a highly experienced Regulatory Affairs professional with exceptionally positive personality. She has specialized experience in managing all kinds of Regulatory and Start-up activities for Clinical Research (across multiple therapeutic areas), Product Registrations, Quality Management, Training Workshops and Conferences for India and South-east Asia. She possess working knowledge of key International Regulations (that of USFDA, EMEA, Health Canada and WHO) for the Pharmaceutical and Clinical Research Industry. Ms. Sneha is a “Certified Trainer” for clinical trials regulatory affairs and corporate behavior. Her academic profile encompasses B. Tech in Biotechnology and Masters in Clinical Research along with a Certificate Course in Intellectual Property Rights (IPR). Also, she has undergone professional trainings/certifications in Schedule-Y and Indian GCP; Good Laboratory Practices (GLP); IPR and TRIPS Agreement; Preparation, Filing and Review of Regulatory documents; Guidelines for Cosmetic Registration and Import and many others. Apart from Regulatory and Study Start-Up Operations Management, her areas of expertise include Quality Control and Internal Quality Audits of Regulatory Documents; Strategic Risk Management and Mitigation Strategies; Client Management & Retention Negotiations; Business development; Training and Development; and Strong Analytical and Content Development Skills. She has attained wealthy proficient experience as a Regulatory affairs professional by serving for 8 years in different organizations like Jubilant Clinsys Pvt. Ltd., Asiatic Clinical Research, Lambda Therapeutic Research; Indian Council of Medical Research; and GVK Bio among others which has eventually helped her develop excellent working relationships at Regulatory Agencies and Scientific Committees. Sneha authored an article titled “Implications of Drugs Going Off Patent” published in magazine “Lifescience India” and has co-authored a chapter on “Anti-Retroviral Medication” for a book on Clinical Pharmacology by Dr. S. D. Seth. She also writes a blog named CheersZindagi.

Ms. Priyanka Kapoor, Senior Faculty Member: A passionate professional working as a Quality assurance and training expert in the field of Clinical Research for the last 7.5 years. Her professional skills include designing and implementing Quality systems within organizations; Performing audits for all Clinical Study phases and BA/BE studies; Preparation and review of SOP's, Protocols; Managing regulatory and sponsor inspection and performing Vendor Qualification Audits. She has gained rich industry exposure from Fortis Clinical Research Ltd, Ranbaxy Research Laboratories and others. Ms. Priyanka has done research work on 'Method development and validation for analysis of molecules on LC-MS/MS extraction procedure' and 'Biological sample analysis for submission of ANDA'. She has also worked as a part of Regulatory Inspection Management Team and faced inspection from FDA, ANVISA, MHRA, WHO etc. Her academic credentials include B. Pharm and M. Pharm (Pharmaceutical Chemistry) with a Post Graduate Diploma in Clinical Research and Pharmacovigilance and Clinical Data

Management. She has two research papers published to her name on “Effect of extract of Zizyphus mauritiana Linn, Root on bacteria causing diarrhoea” in Insian Pharmacist Nov, 2004 and “Pharmacognostical features of Zizyphus mauritiana Linn” in Ancient science of life, Sept 2004.

Dr. Sunita Sharma, Associate Professor: A life science professional, Dr. Sunita Sharma has more than twelve years of research exposure on Industrial pharmaceuticals. Being proficient in diverse areas of strain improvement, process development and fermentation based pharmaceuticals; she has deep interest & vast exposure in GLP/GMP & patent infringement. She also has adequate knowledge of International regulatory guidelines. She has also been associated with Ranbaxy Laboratories Limited as a group leader in the department of fermentation and International Drug Regulatory Affairs. There she has been entrusted with submitting Drug Master Files/Registration Dossiers for in-house manufactured APIs to various regulatory authorities. As per her academic experience, she has worked as a lecturer over three years in the department of microbiology, School of life Sciences, Guru Nanak Dev University, Amritsar. Apart from these, she is also an Ex- Member of Board of studies and Board of control of Microbiology department, Guru Nanak Dev University, Amritsar, India. She has completed her B.Sc, M.Sc and Ph.D. from School of Life Sciences, Guru Nanak Dev University, Amritsar, India.

Dr. Shikha Kumar, Advisor: Dr Shikha Kumar is one of our faculty members and trainers. She has deep interest and vast exposure in GMP training, writing pharma & healthcare related modules and regulatory documents. She has completed her bachelor's in pharmacy from K.N.M.I.P.E.R, Modinagar and her master's in pharmacy from I.T B.H.U, Varanasi. She has also completed her Ph.D from Hamdard University, New Delhi. Apart from these, she is also trained in regulatory affairs and in medical and clinical research writing. She has worked for a couple of pharmaceutical companies i.e. Eli Lilly and Torrent Pharmaceuticals Limited. There she has been entrusted for manuscript writing for non-clinical and clinical studies, compilation of CMC and IMPD for IND filling in UK and India. She has about 15 research articles as an author and about 10 publications as a medical writer in peer-reviewed journals. She has also done patent writing and medical letters writing. During her job in pharma companies, she has also written protocols, investigator's brochure, scientific reports and newsletters for clinical trials. She is fond of writing health related articles and regulatory documents.

Ms. Pooja K. Arora, Advisor: Pooja K Arora, a Healthcare industry professional has acquired her Master's degree in Clinical Research from Cranfield University, UK and professional Diplomas in Pharmaceutical Industry Regulatory Affairs and Pharmaceutical Management from reputed institutes. She has been associated with Clinical Research associate with a few CROs and thus had hands on working basis of the industry. She is presently associated with IGMPI as one of its advisors.

Dr. Snehal Singh, Advisor: Dr. Snehal Singh has a diverse experience of more than 8 years in medical/ scientific/ E-learning and educational writing, which includes good manufacturing practices, clinical research and scientific documents, medico-marketing material, training manuals, E-learning coursem modules, patient education material and educational counseling. She has worked with esteemed organizations like Institute of Preventive Cardiology, Oxygen Healthcare Communications, Satyam BPO and Novartis Healthcare Pvt Ltd. She is a qualified medical professional (B.H.M.S) and has earned Post Graduation in Hospital & Healthcare Management (PGDHHM) and in Preventive & Promotive Health Care (PGDPPHC) on her name. She has also worked as an editor to several health magazines like Health and Wellness, Alternative Medicine, Nutrition and fitness, Pregnancy, Parenting and Child health. She is also experienced in imparting corporate training and training material development.

Ms. Shikha Thakur, Assistant Professor: Shikha Thakur is working with IGMPI as an Assistant Professor. She is responsible for developing training modules e-lectures, personal lectures delivering her best of

knowledge and skills in the domain of Quality Control, Quality Assurance & Good Laboratory Practice.

She is currently also indulged in providing assistance to our senior faculty members in the finalization of training modules' syllabi, content and methodology and conducting e and personal lectures. She is an alumnus of ISF College of Pharmacy, Punjab Technical University, Jalandhar, where she did her Bachelor's and Master's programme in pharmacy with specialization in Quality Assurance. As her remarkable achievement, she is a recipient of DST sponsored PTU fellowship for project entitled “Solubility enhancement of Arteether: Formulation Development and Optimization. She has been entrusted with responsibility of helping advisors and Director General of the Institute in providing the distance cum e-learning and regular participants and trainees with experiential training in the areas of Quality Assurance and Quality Control, Regulatory Affairs, Clinical Research and Good Laboratory Practice.

Ms. Harshita Sharma, Assistant Professor: Currently as an Assistant Professor, Harshita is working on training modules development and co-ordination with an objective of achieving larger mission and goals of the organization. With deep interest and academic excellence in the areas of Pharmaceutics, Quality Assurance & Quality Control, Regulatory Affairs Good Manufacturing Practices and Intellectual Property Rights, she keeps a close watch on latest developments in the Industry. In addition to these responsibilities, she is playing a key role in setting up Project Training division of IGMPI. Harshita has completed B. Pharmacy from Maharaja Surajmal Institute of Pharmacy, IP University, Delhi, and M.Pharmacy with specialization in Pharmaceutics from ISF College of Pharmacy, Punjab Technical University, Jalandhar and is a Ph.D. scholar in the Faculty of Pharmacy, Jamia Hamdard University, New Delhi. Aside from her regular association with IGMPI, she is presently designated as an independent Non-Executive Director in Medicamen Biotech Limited as well.

Ms. Dilrose Pabla, Assistant Professor: Dilrose Pabla has taken up the responsibilities of assisting senior faculty members and advisors of the Institute in development of training modules, e-lectures, training kits, regulatory guidelines etc. Quality Assurance & Quality Control, Regulatory Affairs, Intellectual Property Rights, Nanotechnology & Good Manufacturing Practices are her areas of interest and exploration. She is also playing a key role in organising guest lectures by eminent Industry professionals. Dilrose has completed B. Pharmacy from Sigma Institute of Pharmacy, Gujarat University, Ahmedabad, and M.Pharmacy with specialization in Pharmaceutics from ISF College of Pharmacy, Punjab Technical University, Jalandharand is a Ph.D. scholar in Punjab Technical University.

Ms. Ankita Gururani, Assistant Professor: An industry professional with management experience, Ankita Gururani has been associated with implementation of quality assurance in FMCG sector. She has completed her Bachelors in Medical Microbiology from H.N.B Central University and Masters in Microbiology from Amity University, Noida. Apart from these, she has also acquired acertification on Patent Analyst and has thorough knowledge on IPR, database searches. SWOT, CI, patent portfolio and landscaping. She has also worked with Britannia India Ltd., where she was been entrusted with the responsibility of conducting internal audit programs and implemented QNN and 5S as part of manufacturing excellence. At IGMPI, Ankita has an important role to play in the development of the course content and training modules in the field of food safety and quality assurance with an objective of achieving larger mission and goals of the organization.

Mr. Joshua Martin, Assistant Professor (Food Technology): Joshua has an important role in the development of the course content and training modules. His field of interest is food safety, FSMS, GMP, HAACP & other standards and food packaging. He has a rich exposure to a variety of Food Industries as a consultant in terms of Food Safety. He is an M.Tech in Food Technology with

specialization in Food Process Engineering from SHIATS-DU, Allahabad. Prior to joining IGMPI he was also associated with Nestle. He is a FSSC 22000 certified lead auditor from SGS, India.

Ms. Bhavna Khattar, Programme Co-ordinator: Bhavna's key role is to assist our Advisors in the coordination and execution of our programmes and training modules. She also has good interest in academic deliverables and research in the areas of Good Manufacturing Practices, Quality Assurance and Quality Control, and Regulatory Affairs, IPR etc. She has completed B. Pharmacy from Jaypee University, Solan. Prior to joining IGMPI, she was working with Bioplasma Immunologicals Research.

Ms. Neharika Thakur, Assistant Professor: A logical thinker with immense aptitude for research and development work, Ms. Neharika is a work-driven spirited member of the IGMPI team. She has completed her B.Sc. in Food Technology from Delhi University and M.Sc. in Food Science and Technology from Pondicherry University. Ms. Neharika has qualified UGC NET in Home Science and ICAR NET in Food technology multiple times. Being an active member of the research community, she has authored a few research publications in international journals and her work with “Utilization of deoiled peanut cake in bakery products” is particularly noteworthy. With her sporty spirit and resolution to leave no work incomplete, she is a constant source of inspiration for the students as well as faculty members. Prior to joining IGMPI she has worked as Assistant Professor in ITM University, Gwalior and had research exposure at ICAR institute. At IGMPI, she is involved in lecture delivery and research guidance while conducting interactive sessions with the students.

Ms. Sangita Borah, Assistant Professor: Ms. Sangita is a competent professional with experience in biochemical studies, food quality testing, equipment handling, and research & development. As a part of Faculty of Food Safety and Quality, she is responsible for developing training module, lectures and research in the domain of food processing and technology. She has qualified ICAR-NET in Food technology and her academic credentials include Masters in Food Processing and Technology from Tezpur University, Assam and graduation in Biotechnology from Shillong. She has always been a keen participant of international conferences, seminars, and workshops in the field of food safety and quality improvement of food supply chain. Prior to joining IGMPI, she has worked as Research Analyst in Rai University and Sr. Research Fellow (SRF) in Tezpur University.

Ms. Akanksha Bhandari, Assistant Professor: As a young trainer, known for her vibrant presence and unmatched dedication towards work, She has taken the responsibility of imparting a whole new meaning to IGMPI's resolution of knowledge dissemination. Ms. Bhandari is a B. Pharm, M. Pharm qualified professional from Punjabi University with a Certification in Intellectual Property Rights. She has an impressive hold over the concepts of pharmacovigilance, clinical research, regulatory affairs, good manufacturing practices and is proficient in handling of sophisticated equipments. Her areas of interest include Patent searching, drafting, & writing specifications, Novel drug delivery systems, and Modified release oral dosage forms (Formulation Optimization). Her industrial exposure encompasses IDS Infotech and BRD Medilabs for production and analysis of oral liquids and tablets. Prior to IGMPI, She has worked at Galgotias University, Department of Pharmacy as Assistant Professor.

Ms. Garima Mishra, Assistant Professor: With a good hold over pharma subjects, impressive interaction skills and a sincere learning attitude, Ms. Garima has teamed up with the IGMPI staff in preparation of modules and lecture development. She has keen interest in Organic chemistry, Medicinal Chemistry & Pharmaceutical Analysis and taken lectures on the subjects in reputed pharma colleges. Her industrial exposure encompasses Ranbaxy Laboratories, Akums Pharmaceuticals Pvt. Ltd, Ind-Swift, UNICHEM, Alembic and others. She has completed B. Pharm and M. Pharm (Pharmaceutical Chemistry) during her academic tenure. She has had various research papers

published to her name in Asian Journal of Pharmaceutical and Clinical Research, International Journal of Pharmacy & Life Sciences and International Journal of Medicinal Chemistry and Analysis and many others on the way. She has published a book "Method development and validation by Gas chromatography" and also co-authored "Dissolution Enhancement Using Different Formulation Approaches", Lap Lambert academic publishing (USA).

Ms. Geetanjali Rai, Programme Co-ordinator: Ms. Geetanjali is a highly experienced professional with excellent administrative skills. At IGMPI, she is mainly responsible for setting up effective systems and processes for smooth execution of administration work. She is a multi-tasker with experience in providing Management, Marketing as well as Administrative support to all parts of the work. She is known for a consistent ability to accurately maintain computerized and manual filing/ documentation systems along with answering and resolving queries precisely, in a courteous and confident manner. She has earned proficient skills from her tenure at Max Hospital, Lupin Pharmaceuticals Ltd. and Streatham Place Surgery, London, UK.

Ms. Bhawna Sharma, Research Associate: Bhawna is working with IGMPI in the development of training modules, lectures and assisting the senior faculty members in teaching, training and research. She is having technical competence and interest in the field of Clinical Research, Good Manufacturing Practices and Pharma Product Management. She has completed M. Pharmacy with specialization in Pharmacology from P.D.M. College of Pharmacy, PGIMS University, Haryana and B. Pharmacy from Hindu College of Pharmacy, PGIMS University, Haryana.

Mr. Deepanshu Soni, Technology Officer: With a rich experience in Software Development, Web Development, application development, Deepanshu works as a Technology Officer and is responsible for all the technical works and new initiatives at IGMPI in order to make our Learning Management System (LMS) and other web services to our training participants and students user friendly. He also possesses technical competence and interest in the areas of code development, web design etc. He has completed his B. Tech in Information Technology (I.T) from Vindhya Institute of Technology and Science, R.G.P.V University, Bhopal.

Ms. Rafat Abedi, Director: Rafat Abedi is our Investor & Director. She has been investing in this nonprofit making organization with the primary objective of knowledge dissemination in Good Manufacturing Practices. She looks after administration of IGMPI, training co-ordination, training kits and study materials development and entire logistics for IGMPI. She has previous rich experience in education, training and co-ordination of computer application and management programs.

Mr. Syed S. Abbas, Director: Owing to his academic achievements and interests Syed Abbas has gained work knowledge of several sectors of the business industry, in his career span of twelve years. His contributions to the Pharma and healthcare industries development studies are numerous. Some of

the generous ones count around the esteemed projects, work models, business agendas and organisational setup works he has plotted, guided and worked for in the education and Training Industry, Information Technology industry, Pharmaceutical Research Industry, non-governmental organizations, and many others. He has completed Masters in Public Administration from Lucknow University and Executive MBA from Indian Institute of Management (IIM), Lucknow. He is a member of Indian Pharmaceutical Association (IPA).

As an operations head of IGMPI, he with his experience has been guiding and advising sincerely to bring forth a whole new bouquet of easy learning and training tools for all those using or planning to use or otherwise interested in gaining knowledge about Good Manufacturing Practices.

ADVISORY FACULTY FROM INDUSTRYApart from regular faculty members, eminent and dynamic industrial professionals having rich industrial experience of upto 35-40 years have got associated with IGMPI in regular, part-time, distance cum e-learning and Continuing Education Programme (CEP).The industrial professionals who have joined IGMPI in this initiative have worked in reputed pharmaceutical companies like Ranbaxy Laboratories Ltd,Cadila Pharma Ltd, Dr.Reddy's Laboratories,Quintiles,IPCA, Cipla etc in the areas of GMP,GLP, Clinical Research, QA/QC, IPR, Regulatory Affairs, Drug Discovery, Public Health, Medical Coding etc.The continuing education training programme has been launched with an initiative to provide training to work force in the industry on specific topics in short time period and to quick fix the issues with possible solutions by having an interface with senior industrial professionals.

Post Graduate Diploma in Drug Discovery and DevelopmentThe drug needs are changing rapidly and so is increasing the need of technically and professionally trained individuals with sound knowledge scientific attributes related to the field. The academic training in drug development forms the base but they need to be backed with professionals training. IGMPI serves this purpose well with its distance cum e-learning course in drug development and discovery.

IGMPI course promise to polish the skills of its candidates and make them job ready! The candidates are taught the techniques, given practical knowledge and accustomed to the varied on-field situations that might arise during their careers. All this is made possible with help of:

Extensive course material which has been designed by experts who are or have been contributing to the industry in the past;

Numerous case studies which are a part of the course;

Intelligently aligned course structure which gives step wise knowledge and insight of the industry and all its aspects.

Certified ModulesModule 1 : Fundamentals of Drug Action

Module 2 : Introduction to Drug Discovery and Design

Module 3 : Role of Pharmacology in Drug Discovery

Module 4 : Methods of Drug Discovery and Target Validation

Module 5 : Natural Products as Leads for New Drugs

Module 6 : Pharmacological Screening Models for Therapeutic Areas

Module 7 : Modern Bioanalytical techniques

Module 8 : Biostatistics in Drug Discovery and Development

Module 9 : Combinatorial Chemistry

Module 10 : Quantitative - Structure Activity relationship (QSAR)

Module 11 : Computer Aided Drug Design (CADD)

Module 12 : Demonstration of Instrument Handling used in Pharmaceutical Laboratory

Module 13 : Industry-Based Case Studies

EligibilityAll those who have completed their Graduation are eligible to enroll for the course. As this course is truly professional and industry oriented, individuals having experience in any sector (production, processing, quality, trial, R&D etc.) in the Pharma, food and healthcare industry (Drugs manufacturing , Medical Device, Ayurvedic, Pharmaceutical Industry Regulation, Clinical Research, Homeopathic or Ayurvedic Medicine Manufacturing, Cosmetic Manufacturing, Food manufacturing, Food Ingredient and Additive processing, Biotechnology) can also seek benefits of the course.

Programme DurationMinimum time in which a student can complete this diploma course is one year while a maximum of two consecutive years is allowed to complete the course.

Programme DeliverablesA comprehensive study material for all the modules in hard copies ensuring the needs of the audience. The accompanying training material is appropriately aligned with the current Industry’s expectations.

Assignments for all the programme modules for continuous evaluation and guidance.

Interactive or recorded lectures on all key areas of the programme giving all flexibility to the participants.

Assessment and evaluation for all the programme modules in order to enhance the levels of competencies and skills of the participants leading towards the objective of application in the job. .

At the end of each programme modules, the trainers shall obtain feedback from the participants using specially designed questionnaires.

All learning and training delivery initiatives shall be conducted in English.

Registration The registration dates for this bi-annual programme run by the institute are updated timely on the webpage. Effective E-learning tools incorporated into the design of the webpage make the course lectures, videos and study material easily accessible. This gives huge window of self-regulated and self-paced performance to the participants.

Examination & CertificationAll the participants are expected to appear for an online exam and are also obliged to submit assignments after each module. After successful completion, the participants will be awarded Post Graduate Diploma in Drug Discovery and Development. For all the above mentioned modules elaborate course material, self-assessment assignments and project work details would be provided by the Institute from time to time. Details get updated on the webpage as well. This programme is approved by Quality Council Of India.

Placement Assistance & Corporate RelationsIGMPI offers placement assistance to its students. The Institute has partnered with many organizations for providing placement assistance to its participants. Besides, it has a robust placement cell comprising senior level Human Resources professionals and Talent Acquisition experts which maintain close links with business industry. This cell is continuously engaged in promoting employability of our participants. The efforts of our placement cell also include helping with professional resume writing while also assisting assessing them to polish their interview skills.

In recent months the Institute has witnessed more and more participation from professionals working with global pharmaceutical, healthcare and food giants like Dr. Reddy's Laboratories, Aurobindo

Pharma, Glenmark Generics, Cipla, Wockhardt, Pfizer, Abbott, Medtronic, Foster Corporation, Ipca Laboratories, Calyx, Mother Dairy, Bliss GVS Pharma, Al Rawabi, Almarai, Green Pastures, Accenture, Wipro, Fortis Clinical Research, Quintiles, SeQuent, PepsiCo India, Mankind, Beryl Drugs, CFTRI, Ciron, Sun Pharmaceutical, Novartis, GlaxoSmithKline, Biocon, Apollo Hospitals, etc.

Executive Diploma in Drug Discovery and DevelopmentDrug discovery and development needs multidisciplinary skills to excel and the IGMPI taps this need by introducing its new distance cum e-learning Executive Diploma Course in Drug Discovery and Development.

While interest in the field comes as an integral part of the aspiring candidate's nature, rest of the skills and knowledge can be built upon by effectively designed courses. The multidisciplinary team at IGMPI has targeted to add to the pool of efficient public health professionals they ought to achieve it through this distance cum e-learning Executive Diploma Course in Drug Discovery and Development.

The case study based approach in Executive Diploma programme via distance cum e learning mode is designed for working professionals in full-time employment who wish to complete the course in shorter time duration. This course is beneficial for professionals from different streams to help them intensify their knowledge. This is a fast track and advanced course having rigorous case studies based methodology throughout the duration.

Certified ModulesModule 1 : Fundamentals of Drug Action

Module 2 : Introduction to Drug Discovery and Design

Module 3 : Role of Pharmacology in Drug Discovery

Module 4 : Methods of Drug Discovery and Target Validation

Module 5 : Natural Products as Leads for New Drugs



Module 8 : Biostatistics in Drug Discovery and Development

Module 9 : Combinatorial Chemistry

Module 10 : Quantitative - Structure Activity relationship (QSAR)

Module 11 : Computer Aided Drug Design (CADD)

Module 12 : Demonstration of Instrument Handling used in Pharmaceutical Laboratory

Module 13 : Industry-Based Case Studies

EligibilityAll those working in the Pharmaceutical Industry or any sector of Healthcare industry or any other industry type (India or abroad) can apply for this short term programme. Life Science Graduate/ diploma holders are eligible for the course. Working professionals of any of the following industry types; Drugs manufacturing , Medical Device, Ayurveda, Pharmaceutical Industry Regulation, Clinical Research, Homeopathic or Ayurveda Medicine Manufacturing, Cosmetic Manufacturing, Food manufacturing, Food Ingredient and Additive processing, Biotechnology or any related industry are

highly encouraged to apply for the programme.

Programme DurationMinimum time in which a student can complete this diploma course is 6 months while a maximum of 12 months is allowed to complete the course.







RegistrationThe registration dates for this bi-annual programme run by the institute are updated timely on the webpage.

Examination & CertificationAll the participants are expected to appear for an online exam and are also obliged to submit assignments after each module. After successful completion, the participants will be awarded Executive Diploma in Drug Discovery and Development. For all the above mentioned modules elaborate course material, self-assessment assignments and project work details would be provided by the Institute from time to time. Details get updated on the webpage as well. This programme is approved by Quality Council Of India.

Placement Assistance & Corporate Relations IGMPI offers placement assistance to its students. The Institute has partnered with many organizations for providing placement assistance to its participants. Besides, it has a robust placement cell comprising senior level Human Resources professionals and Talent Acquisition experts which maintain close links with business industry. This cell is continuously engaged in promoting employability of our participants. The efforts of our placement cell also include helping with professional resume writing while also assisting assessing them to polish their interview skills.

In recent months the Institute has witnessed more and more participation from professionals working with global pharmaceutical, healthcare and food giants like Dr. Reddy's Laboratories, Aurobindo Pharma, Glenmark Generics, Cipla, Wockhardt, Pfizer, Abbott, Medtronic, Foster Corporation, Ipca

Laboratories, Calyx, Mother Dairy, Bliss GVS Pharma, Al Rawabi, Almarai, Green Pastures, Accenture, Wipro, Fortis Clinical Research, Quintiles, SeQuent, PepsiCo India, Mankind, Beryl Drugs, CFTRI, Ciron, Sun Pharmaceutical, Novartis, GlaxoSmithKline, Biocon, Apollo Hospitals, etc

There is a huge demand of Drug Discovery and Development Professionals in the Pharmaceutical and Chemical industry today!Professionals in this industry have a global standing and responsibility as well. The work done here serves to global audience and is not just country specific. Thus, the field beholds immense respect for its takers which comes with equal amounts of pressure to ensure proper code and ethics of the field are followed. IGMPI offers comprehensive training in drug discovery and development which is essential; for ensuring a benefitting future in the industry. Pass outs from this course are eligible to find work in:

Pharmaceutical companies,

Biomedical companies,

Technology/consulting companies in the healthcare arena or even government sector

The course also prepares for positions and roles like Medicinal chemist, Computational chemist, Nano Technician or In Silico Drug Designer. IGMPI offers professional and industry oriented training thus opening doors for entry into the industry. PG diploma in Drug discovery and Development adds advantage for those already in the industry as a tag of professional training and those new to the industry feel comfortable with backing of apt and up-to-date information and training required to have sustained growth in the industry.

Post Graduate Diploma in Pharmaceutical ChemistryThe field of pharmaceutical chemistry arises from the combination of synthetic organic chemistry with pharmacology and medicinal sciences. It encompasses the design, chemical synthesis and development of active pharmaceutical ingredients (APIs), or bio-active molecules. It enables a student to have a detailed knowledge of the chemical aspects of identification, followed by systematic, thorough synthetic alteration of new chemical entities to make them suitable for therapeutic use. It includes synthetic and computational aspects of the study of existing drugs and agents in development in relation to their bioactivities (biological activities and properties), i.e., understanding their structure-activity relationships (SAR). Pharmaceutical chemistry is focused on quality aspects of medicines and aims to assure fitness for purpose of medicinal products.

Pharmaceutical chemists apply their chemistry training to the process of synthesizing new pharmaceuticals. They also improve the processes by which existing pharmaceuticals are made. Pharmaceutical chemists are focused on drug discovery and development and are concerned with the isolation of medicinal agents found in plants, as well as the creation of new synthetic drug compounds. Thus Pharmaceutical chemistry is a versatile and stimulating field as it links many scientific disciplines and allows for collaboration with other scientists in researching and developing new drugs.

The Post Graduate Diploma in Pharmaceutical Chemistry has been structured by experts from the industry themselves and thus comprehensive coverage and understanding of the industry and its functional areas is promised. The goal of the Post Graduate Diploma Programme is to familiarize the participant with the updated theoretical and practical aspects of the Medicinal Chemistry to gain access to this challenging and interesting field.

Certified ModulesModule 1 : Advanced Organic Chemistry-1

Module 2 : Advanced Organic Chemistry-2

Module 3 : Modern Analytical Techniques

Module 4 : Medicinal Chemistry

Module 5 : Chemistry of Natural Products

Module 6 : Basics of Drug Discovery and Design

Module 7 : Drug Discovery and Target Validation



Module 10 : Basics of Computer Aided Drug Design (CADD)

Module 11 : Technique of Combinatorial Chemistry

Module 12 : Importance of Quantitative – Structure Activity relationship (QSAR)

Module 13 : Biostatistics in Pharmaceutical Chemistry

Module 14 : Laboratory demonstration of Pharmaceutical Chemistry practicals and Instrument Handling

EligibilityAll those who have completed their Graduation are eligible to enroll for the course. As this course is

truly professional and industry oriented, individuals having experience in any sector (production, processing, quality, trial, R&D etc.) in the Pharma, food and healthcare industry (Drugs manufacturing, Medical Device, Ayurvedic, Pharmaceutical Industry Regulation, Clinical Research, Homeopathic or Ayurvedic Medicine Manufacturing, Cosmetic Manufacturing, Food manufacturing, Food Ingredient and Additive processing, Biotechnology) can also seek benefits of the course.

Programme DurationMinimum duration to complete this program is 1 year and maximum is 2 years







RegistrationThe registration dates for this bi-annual executive program run by the institute are updated timely on the webpage. The Training sessions and webinars are strictly scheduled depending on the availability of speakers. Effective E-learning tools incorporated into the design of the webpage make the course lectures, videos and study material easily accessible. This gives huge window of self-regulated and self-paced performance to the participants.

Examination & CertificationAll the participants are expected to appear for an online exam and are also obliged to submit assignments after each module. After successful completion, the participants will be awarded Post Graduate Diploma in Pharmaceutical Chemistry. For all the above mentioned modules elaborate course material, self-assessment assignments and project work details would be provided by the Institute from time to time. Details get updated on the webpage as well.

Placement Assistance & Corporate RelationsThe Institute has partnered with many organizations for providing with placement assistance to in its participants. Besides, it has a robust placement cell comprised of senior level Human Resources professionals and Talent Acquisition experts which maintains close links with business and industry. This cell is continuously engaged in promoting the employability of our participants and encouraging the concerned Human Resources department and Hiring Managers to recruit/hire our participants for their vacant positions. The efforts of our placement cell also include helping with professional resume

writing & interview skills.

In recent months the Institute has witnessed more and more participation from professionals working with global pharmaceutical, healthcare and food giants like Dr. Reddy's Laboratories, Aurobindo Pharma, Glenmark Generics, Cipla, Wockhardt, Pfizer, Abbott, Medtronic, Foster Corporation, Ipca Laboratories, Calyx, Mother Dairy, Bliss GVS Pharma, Al Rawabi, Almarai, Green Pastures, SeQuent, PepsiCo India, Mankind, Beryl Drugs, Allergy Therapeutics, CFTRI, Ciron, Sun Pharmaceutical, Novartis, GlaxoSmithKline, Ranbaxy, Biocon etc.

Executive Diploma in Pharmaceutical ChemistryThis short term programme has been designed mainly to provide knowledge of the fundamentals of Pharmaceutical chemistry and drug design very comprehensively. The programme provides overview of practical situations and case studies along with details of new practices and techniques. Thus it works as re-fresher course for those already in the industry and an insight or practical guide for those planning to enter into this sector.

Certified ModulesModule 1 : Advanced Organic Chemistry-1

Module 2 : Advanced Organic Chemistry-2

Module 3 : Modern Analytical Techniques

Module 4 : Medicinal Chemistry

Module 5 : Chemistry of Natural Products

Module 6 : Basics of Drug Discovery and Design




Module 10 : Basics of Computer Aided Drug Design (CADD)

Module 11 : Technique of Combinatorial Chemistry

Module 12 : Importance of Quantitative – Structure Activity relationship (QSAR)

Module 13 : Biostatistics in Pharmaceutical Chemistry

Module 14 : Laboratory demonstration of Pharmaceutical Chemistry practicals and Instrument Handling

EligibilityAll those working in the Pharmaceutical Industry or any sector of Healthcare industry or any other industry type (India or abroad) can apply for this short term programme. Life Science Graduate/ diploma holders are eligible for the course. Working professionals of any of the following industry types; Drugs manufacturing , Medical Device, Ayurveda, Pharmaceutical Industry Regulation, Clinical Research, Homeopathic or Ayurveda Medicine Manufacturing, Cosmetic Manufacturing, Food manufacturing, Food Ingredient and Additive processing, Biotechnology or any related industry are highly encouraged to apply for the programme.

Programme DurationMinimum duration to complete this programme is 6 months and maximum is 12 months







RegistrationThe registration dates for this bi-annual executive programme run by the institute are updated timely on the webpage. The Training sessions and webinars are strictly scheduled depending on the availability of speakers. Effective E-learning tools incorporated into the design of the webpage make the course lectures, videos and study material easily accessible. This gives huge window of self-regulated and self-paced performance to the participants.

Examination & CertificationAll the participants are expected to appear for an online exam and are also obliged to submit assignments after each module. After successful completion, the participants will be awarded Executive Diploma in Pharmaceutical Chemistry. For all the above mentioned modules elaborate course material, self-assessment assignments and project work details would be provided by the Institute from time to time. Details get updated on the webpage as well.

Placement Assistance & Corporate Relations The Institute has partnered with many organizations for providing with placement assistance to in its participants. Besides, it has a robust placement cell comprised of senior level Human Resources professionals and Talent Acquisition experts which maintains close links with business and industry. This cell is continuously engaged in promoting the employability of our participants and encouraging the concerned Human Resources department and Hiring Managers to recruit/hire our participants for their vacant positions. The efforts of our placement cell also include helping with professional resume writing & interview skills.

In recent months the Institute has witnessed more and more participation from professionals working with global pharmaceutical, healthcare and food giants like Dr. Reddy's Laboratories, Aurobindo

Pharma, Glenmark Generics, Cipla, Wockhardt, Pfizer, Abbott, Medtronic, Foster Corporation, Ipca Laboratories, Calyx, Mother Dairy, Bliss GVS Pharma, Al Rawabi, Almarai, Green Pastures, SeQuent, PepsiCo India, Mankind, Beryl Drugs, Allergy Therapeutics, CFTRI, Ciron, Sun Pharmaceutical, Novartis, GlaxoSmithKline, Biocon etc.

There is a huge demand of Pharmaceutical chemists in Healthcare industry today!Pharmaceutical chemistry offers a wide variety of opportunities in pharmaceutical, biotechnology, and medical device companies. Most chemists use their research skills to formulate, produce, characterize, and analyze new compounds for specific applications. The professionals in the field can also assume regulatory positions like reviewing drug applications at the regulatory bodies.

The pharmaceutical chemists are mainly involved in finding new cures and discovering new molecules through a wide variety of techniques like CADD, high-throughput screening, combinatorial chemistry etc. Many medicinal chemists start out in the lab and then move on to other laboratory career such as process chemistry, formulation chemistry, quality control or quality assurance. They may also move to nonlaboratory careers such as regulatory affairs, intellectual property (patents), project management, or technology transfer.

Careers in this Field

Basic research into how various chemicals affect biological systems

Drug development, including formulating drugs used to treat patients with diseases

Testing potential new bio-active compounds in patient populations

Developing guidelines for how new pharmaceuticals will be such as chemists at the regulatory bodies who review new drug applications from pharmaceutical companies and the processes by which the substances are made

Post Graduate Diploma in BioinformaticsBioinformatics is an interdisciplinary field that develops methods and software tools for understanding biological data. As an interdisciplinary field of science, bioinformatics combines computer science, statistics, mathematics, and engineering to analyze and interpret biological data. It is a new emerging field that helps in collecting, linking, and manipulating different types of biological information to discover new biological insight. This programme is targeted towards imparting theoretical as well as practical knowledge of bioinformatics to its participants. After completion of the course participant is expected to have in-depth knowledge and better understanding of sequence analysis, prediction of protein structure, genome annotation, comparative genomics, health and drug discovery, microarray profiling. The modules have been compiled to introduce the attendee to various aspects of bioinformatics, its need and benefits in biological research.

Certified ModulesModule 1 : Introduction to bioinformatics

Module 2 : Biological databases and data generation

Module 3 : Biostatistics I

Module 4 : Biostatistics II

Module 5 : Biomolecules

Module 6 : Cell biology and genetics

Module 7 : Molecular biology

Module 8 : Structural bioinformatics and drug discovery

Module 9 : Concepts and Principle of 2D and 3D QSARModule 10 : Computational Molecular Biology and Computational toolsModule 11 : Bioprogramming and Bioinformatics SoftwaresModule 12 : Introduction to Big Data AnalyticsModule 13 : Pharmaceutical and Healthcare Data Management

Module 14 : Implementation of Big Data Analytics in Pharmaceuticals and Healthcare Industry

EligibilityAny Indian or oversees applicants must fulfil following criteria for enrolling into the one year Bioinformatics program. The applicant must be a Graduate in B.Sc in Biology or B.Sc in Maths/Statistics with biology in 10+2 as one of the subjects.

Programme DurationMinimum duration to complete this program is 1 year and maximum is 2 years.




Assessment and evaluation for all the programme modules in order to enhance the levels of competencies and skills of the participants leading towards the objective of application in the job.




Examination & CertificationAll the participants are expected to appear for an online exam and are also obliged to submit assignments after each module. After successful completion, the participants will be awarded Post Graduate Diploma in Bioinformatics. For all the above mentioned modules elaborate course material, self-assessment assignments and project work details would be provided by the Institute from time to time. Details get updated on the webpage as well.

Placement Assistance & Corporate RelationsThe Institute has partnered with many organizations for providing with placement assistance to in its participants. Besides, it has a robust placement cell comprised of senior level Human Resources professionals and Talent Acquisition experts which maintains close links with business and industry. This cell is continuously engaged in promoting the employability of our participants and encouraging the concerned Human Resources department and Hiring Managers to recruit/hire our participants for their vacant positions. The efforts of our placement cell also include helping with professional resume writing & interview skills.


Future career prospects of BioinformaticsCurrent biological and medical labs use methods that produce extremely large data sets, which cannot be analyzed by hand - for instance sequencing human genomes. Thus modern biological and medical research and development cannot be done without bioinformatics. Future applications in biology, chemistry, pharmaceuticals, medicine, and agriculture. In addition, bioinformatics plays an important role in biomedical research. Research work in the area of genetic diseases and medical genomics is rapidly increasing and the future of personalized medicine depends on bioinformatics approaches.

Executive Diploma in Bioinformatics This short term programme has been designed mainly to provide brief of Bioinformatics. The programme provides collecting, linking, and manipulating different types of biological information to discover new biological insight. Thus it works as re-fresher course for those already in the industry and an insight or practical guide for those planning to enter into this sector. You can complete this course from your own city.

Certified ModulesModule 1 : Introduction to bioinformatics

Module 2 : Biological databases and data generation

Module 3 : Biostatistics I

Module 4 : Biostatistics II

Module 5 : Biomolecules

Module 6 : Cell biology and genetics

Module 7 : Molecular biology

Module 8 : Structural bioinformatics and drug discovery

Module 9 : Concepts and Principle of 2D and 3D QSARModule 10 : Computational Molecular Biology and Computational toolsModule 11 : Bioprogramming and Bioinformatics SoftwaresModule 12 : Introduction to Big Data AnalyticsModule 13 : Pharmaceutical and Healthcare Data Management

Module 14 : Implementation of Big Data Analytics in Pharmaceuticals and Healthcare Industry

EligibilityAny Indian or oversees applicants must fulfil following criteria for enrolling into the one year Bioinformatics program. The applicant must be a Graduate in B.Sc in Biology or B.Sc in Maths/Statistics with biology in 10+2 as one of the subjects.

Programme DurationMinimum duration to complete this program is 6 Months while a maximum of one year is allowed to complete the course.




Assessment and evaluation for all the programme modules in order to enhance the levels of competencies and skills of the participants leading towards the objective of application in the job. At the end of each programme modules, the trainers shall obtain feedback from the participants using specially designed questionnaires.



Examination & CertificationAll the participants are expected to appear for an online exam and are also obliged to submit assignments after each module. After successful completion, the participants will be awarded Executive Diploma in Bioinformatics. For all the above mentioned modules elaborate course material, self-assessment assignments and project work details would be provided by the Institute from time to time. Details get updated on the webpage as well.



Future career prospects of BioinformaticsCurrent biological and medical labs use methods that produce extremely large data sets, which cannot be analyzed by hand - for instance sequencing human genomes. Thus modern biological and medical research and development cannot be done without bioinformatics. Future applications in biology, chemistry, pharmaceuticals, medicine, and agriculture. In addition, bioinformatics plays an important role in biomedical research. Research work in the area of genetic diseases and medical genomics is rapidly increasing and the future of personalized medicine depends on bioinformatics approaches.

Post Graduate Diploma in Pharmaceutical Formulation and EntrepreneurshipAll Pharmaceutical products are formulated to specific dosage forms for drugs to be effectively delivered to patients. Different dosage forms require different pharmaceutical technologies and usually present different technical challenges for formulation development. The objective of this course is to provide fundamentals of formulation studies and how the physiochemical, physiomechanical and biopharmaceutical properties effect the dosage development.

This programme provides professionals with the skills and knowledge to allow them to participate effectively in the creation and growth of high impact pharmaceutical business ventures. The development of this course is in direct response to the demands of industry and its professionals will be highly competitive in the global jobs market

Certified ModulesModule 1 : Introduction to Formulation

Development and PreformulationStudies

Module 2 : Pharmaceutical Additives and Polymers

Module 3 : Formulation of Biphasic Liquid DosageForms, Semi-solid Dosage Forms andParenteral Products

Module 4 : Pharmaceutical Aerosols and VeterinaryDosage Forms

Module 5 : Formulation of Solid and Liquid DosageForms

Module 6 : Molecular Pharmaceutics(Nanotechnology and Targeted DDS)

Module 7 : Controlled and Sustained Released dosage Forms

Module 8 : Drug Stability and Pharmaceutical Packaging

Module 9 : Optimization Techniques and Computer aided Drug formulation

Module 10 : Cosmeceuticals and Neutraceuticals

Module 11 : Bioavailability and Bioequivalence studies

Module 12 : Laboratory Demonstration of Formulation Development of Dosage forms and their Evaluation

Module 13 : Pharmaceutical Marketing Management and Entrepreneual Marketing

Module 14 : Pharmacoeconomics

Module 15 : Business Strategy

Module 16 : Initiating Pharmaceutical Start Up

Module 17 : Industry based Case Studies

EligibilityAll those who have completed their Graduation or Post Graduation/ Pharma / PhD are eligible to enroll

for the course. As this course is truly professional and industry oriented, employed individuals working in any sector (production, processing, quality, trial, R&D etc.) in the healthcare industry (Food manufacturing, Food Ingredient and Additive processing, Drugs manufacturing , Medical Device, Ayurveda, Pharmaceutical Industry Regulation, Clinical Research, Homeopathic or Ayurveda Medicine Manufacturing, Cosmetic Manufacturing, Biotechnology) can also seek benefits of the course.









Examination & CertificationAll the participants are expected to appear for an online exam and are also obliged to submit assignments after each module. After successful completion, the participants will be awarded Post Graduate Diploma in Pharmaceutical Formulation and Entrepreneurship. For all the above mentioned modules elaborate course material, self-assessment assignments and project work details would be provided by the Institute from time to time. Details get updated on the webpage as well.

Placement Assistance & Corporate RelationsThe Institute has partnered with many organizations for providing with placement assistance to in its participants. Besides, it has a robust placement cell comprised of senior level Human Resources professionals and Talent Acquisition experts which maintains close links with business and industry. This cell is continuously engaged in promoting the employability of our participants and encouraging the concerned Human Resources department and Hiring Managers to recruit/hire our participants for

their vacant positions. The efforts of our placement cell also include helping with professional resume writing & interview skills.

In recent months the Institute has witnessed more and more participation from professionals working with global pharmaceutical, healthcare and food giants like Dr. Reddy’s Laboratories, Aurobindo Pharma, Glenmark Generics, Cipla, Wockhardt, Pfizer, Abbott, Medtronic, Foster Corporation, Ipca Laboratories, Calyx, Mother Dairy, Bliss GVS Pharma, Al Rawabi, Almarai, Green Pastures, SeQuent, PepsiCo India, Mankind, Beryl Drugs, Allergy Therapeutics, CFTRI, Ciron, Sun Pharmaceutical, Novartis, GlaxoSmithKline, Ranbaxy, Biocon etc.

Future career prospects of Pharmaceutical Formulation and EntrepreneurshipFormulation science is a hands-on career. Formulation chemists are needed not only in the innovator and generic pharmaceutical industries products, but also for all sorts of chemical products including pesticides and insecticides, paints and coatings, foods, adhesives, cosmetics, fragrances, and many household products.

Formulation professionals work in a wide variety of industries. They may divide their time testing new formulations in the lab, writing reports, and helping to set up new production facilities in a pilot plant. After completion of the course professionals will have the necessary skills to start-up new businesses in pharmaceutical formulation or join the pharmaceutical industry's formulation development team.

Executive Diploma in Pharmaceutical Formulation and EntrepreneurshipThis short term programme has been designed mainly to provide brief of Pharmaceutical Formulation and Development. The programme provides collecting, linking, and manipulating different types of biological information to discover new biological insight. Thus it works as re-fresher course for those already in the industry and an insight or practical guide for those planning to enter into this sector. You can complete this course from your own city.

Certified ModulesModule 1 : Introduction to Formulation Development and Preformulation StudiesModule 2 : Pharmaceutical Additives and PolymersModule 3 : Formulation of Biphasic Liquid Dosage Forms, Semi-solid Dosage Forms and Parenteral ProductsModule 4 : Pharmaceutical Aerosols and Veterinary Dosage FormsModule 5 : Formulation of Solid and Liquid Dosage FormsModule 6 : Molecular Pharmaceutics (Nanotechnology and Targeted DDS)Module 7 : Controlled and Sustained Released dosage FormsModule 8 : Drug Stability and Pharmaceutical PackagingModule 9 : Optimization Techniques and Computer aided Drug formulationModule 10 : Cosmeceuticals and NeutraceuticalsModule 11 : Bioavailability and Bioequivalence studiesModule 12 : Laboratory Demonstration of Formulation Development of Dosage forms and their EvaluationModule 13 : Pharmaceutical Marketing Management and Entrepreneual MarketingModule 14 : PharmacoeconomicsModule 15 : Business StrategyModule 16 : Initiating Pharmaceutical Start UpModule 17 : Industry based Case Studies

EligibilityAll those who have completed their Graduation or Post Graduation/ Pharma / PhD are eligible to enrol for the course. As this course is truly professional and industry oriented, employed individuals working in any sector (production, processing, quality, trial, R&D etc.) in the healthcare industry (Food manufacturing, Food Ingredient and Additive processing, Drugs manufacturing , Medical Device, Ayurveda, Pharmaceutical Industry Regulation, Clinical Research, Homeopathic or Ayurveda Medicine Manufacturing, Cosmetic Manufacturing, Biotechnology) can also seek benefits of the course.









Examination & CertificationAll the participants are expected to appear for an online exam and are also obliged to submit assignments after each module. After successful completion, the participants will be awarded Executive Diploma in Pharmaceutical Formulation and Entrepreneurship. For all the above mentioned modules elaborate course material, self-assessment assignments and project work details would be provided by the Institute from time to time. Details get updated on the webpage as well.


In recent months the Institute has witnessed more and more participation from professionals working with global pharmaceutical, healthcare and food giants like Dr. Reddy’s Laboratories, Aurobindo Pharma, Glenmark Generics, Cipla, Wockhardt, Pfizer, Abbott, Medtronic, Foster Corporation, Ipca Laboratories, Calyx, Mother Dairy, Bliss GVS Pharma, Al Rawabi, Almarai, Green Pastures, SeQuent, PepsiCo India, Mankind, Beryl Drugs, Allergy Therapeutics, CFTRI, Ciron, Sun Pharmaceutical, Novartis, GlaxoSmithKline, Ranbaxy, Biocon etc.

Future career prospects of Pharmaceutical Formulation and EntrepreneurshipFormulation science is a hands-on career. Formulation chemists are needed not only in the innovator and generic pharmaceutical industries products, but also for all sorts of chemical products including pesticides and insecticides, paints and coatings, foods, adhesives, cosmetics, fragrances, and many household products.

Formulation professionals work in a wide variety of industries. They may divide their time testing new formulations in the lab, writing reports, and helping to set up new production facilities in a pilot plant.

Post Graduate Diploma in Herbal Drug TechnologyHerbal Drug Technology is the study of drugs of natural origin. Herbal medicines have been widely used all over the world since ancient times by physicians and patient for their better therapeutic value as they have no or less side effects as compared with modern medicines. The resurgence of herbal medicine demands for studies in this field. It includes quality control, efficacy and safety of herbal drugs and medicaments.

This course will provide professionals with the good basic grounding of physical, chemical, biochemical and biological properties of drug substances or potential drugs of natural origin as well as the search of new drugs from natural sources.

Certified ModulesModule 1 : Introduction to Herbal Drug TechnologyModule 2 : Indian System of MedicineModule 3 : Medicinal BotanyModule 4 : Modern Analytical Techniques Module 5 : Tissue Culture of Medicinal PlantsModule 6 : Extraction, Isolation and Analysis of PhytopharmaceuticalsModule 7 : Screening and Standardization of Herbal drugsModule 8 : Herbal FormulationsModule 9 : Herbal CosmeticsModule 10 : NutraceuticalsModule 11 : Quality Control of Herbal DrugsModule 12 : WHO and ICH Guidelines for Herbal DrugsModule 13 : Herbal drugs: Standards, Regulation and PatentingModule 14 : Good Manufacturing Practices for Herbal drugs

EligibilityAll those who have completed their Graduation or Post Graduation in Life Sciences are eligible to enroll for the course. As this course is truly professional and industry oriented, employed individuals working in any sector (production, processing, quality, trial, R&D etc.) in the healthcare industry (Food manufacturing, Food Ingredient and Additive processing, Drugs manufacturing , Medical Device, Ayurveda, Pharmaceutical Industry Regulation, Clinical Research, Homeopathic or Ayurveda Medicine Manufacturing, Cosmetic Manufacturing, Biotechnology) can also seek benefits of the course.









Examination & CertificationAll the participants are expected to appear for an online exam and are also obliged to submit assignments after each module. After successful completion, the participants will be awarded Post Graduate Diploma in Herbal Drug Technology. For all the above mentioned modules elaborate course material, self-assessment assignments and project work details would be provided by the Institute from time to time. Details get updated on the webpage as well.


In recent months the Institute has witnessed more and more participation from professionals working with global pharmaceutical, healthcare and food giants like Dr. Reddy Laboratories, AurobindoPharma, Glenmark Generics, Cipla, Wockhardt, Pfizer, Abbott, Medtronic, Foster Corporation, Ipca Laboratories, Calyx, Mother Dairy, Bliss GVS Pharma, Al Rawabi, Almarai, Green Pastures, SeQuent, PepsiCo India, Mankind, Beryl Drugs, Allergy Therapeutics, CFTRI, Ciron, Sun Pharmaceutical, Novartis, GlaxoSmithKline, Ranbaxy, Biocon etc.

Future career prospects of Herbal Drug TechnologyBefore complex medicinal chemistry was developed, people used remedies created by the simple tools and ingredients afforded to them by nature. After completion of this course professionals will have knowledge of how to use various parts of plants, including seeds, roots and bark to create medication, herbal supplements and natural dietary aids.

This course will help professionals to get job in Production, Manufacturing, Research & Development and Marketing of herbal medicines. They also have plenty of opportunities in specialized fields such as herbal medicine, Acupuncture, Naturopathy etc.

Executive Diploma in Herbal Drug TechnologyThis short term programme has been designed mainly to provide brief of Herbal Drug Technology. The programme provides collecting, linking, and manipulating different types of biological information to discover new biological insight. Thus it works as re-fresher course for those already in the industry and an insight or practical guide for those planning to enter into this sector. You can complete this course from your own city.

Certified ModulesModule 1 : Introduction to Herbal Drug TechnologyModule 2 : Indian System of MedicineModule 3 : Medicinal BotanyModule 4 : Modern Analytical Techniques Module 5 : Tissue Culture of Medicinal PlantsModule 6 : Extraction, Isolation and Analysis of PhytopharmaceuticalsModule 7 : Screening and Standardization of Herbal drugsModule 8 : Herbal FormulationsModule 9 : Herbal CosmeticsModule 10 : NutraceuticalsModule 11 : Quality Control of Herbal DrugsModule 12 : WHO and ICH Guidelines for Herbal DrugsModule 13 : Herbal drugs: Standards, Regulation and PatentingModule 14 : Good Manufacturing Practices for Herbal drugs

EligibilityAll those who have completed their Graduation or Post Graduation in Life Sciences are eligible to enroll for the course. As this course is truly professional and industry oriented, employed individuals working in any sector (production, processing, quality, trial, R&D etc.) in the healthcare industry (Food manufacturing, Food Ingredient and Additive processing, Drugs manufacturing , Medical Device, Ayurveda, Pharmaceutical Industry Regulation, Clinical Research, Homeopathic or Ayurveda Medicine Manufacturing, Cosmetic Manufacturing, Biotechnology) can also seek benefits of the course.









Examination & CertificationAll the participants are expected to appear for an online exam and are also obliged to submit assignments after each module. After successful completion, the participants will be awarded Executive Diploma in Herbal Drug Technology. For all the above mentioned modules elaborate course material, self-assessment assignments and project work details would be provided by the Institute from time to time. Details get updated on the webpage as well.


In recent months the Institute has witnessed more and more participation from professionals working with global pharmaceutical, healthcare and food giants like Dr. Reddy Laboratories, AurobindoPharma, Glenmark Generics, Cipla, Wockhardt, Pfizer, Abbott, Medtronic, Foster Corporation, Ipca Laboratories, Calyx, Mother Dairy, Bliss GVS Pharma, Al Rawabi, Almarai, Green Pastures, SeQuent, PepsiCo India, Mankind, Beryl Drugs, Allergy Therapeutics, CFTRI, Ciron, Sun Pharmaceutical, Novartis, GlaxoSmithKline, Ranbaxy, Biocon etc.

Future career prospects of Herbal Drug TechnologyBefore complex medicinal chemistry was developed, people used remedies created by the simple tools and ingredients afforded to them by nature. After completion of this course professionals will have knowledge of how to use various parts of plants, including seeds, roots and bark to create medication, herbal supplements and natural dietary aids.

This course will help professionals to get job in Production, Manufacturing, Research & Development and Marketing of herbal medicines. They also have plenty of opportunities in specialized fields such as herbal medicine, Acupuncture, Naturopathy etc.

Post Graduate Diploma in Pharmaceutical Process EngineeringPharmaceutical Process engineers are involved in the planning, conception, design, construction/Execution, management, operation of research facilities, pilot plant for scale up, manufacturing plants and labelling & packaging processes in the conversion of chemical and biological materials into valuable pharmaceuticals and pharmaceutical therapies. They have to implement FDA regulations, validation assurance, quality control, and maintain Good Manufacturing Practices (GMP) compliant facilities. In addition to the safety of the end product, they have to maintain a level of personal and environmental safety.

The processes that they come up with are used to create products ranging from oil, gas& drugs to food and drink.

This course will provide a thorough understanding of Process engineering in API and in formulation for develop and design new process and modify existing ones in very cost effective way with safety, increase productivity in existing system, engineering calculations for taking decision at spot etc. This course provides professionals with the skills and knowledge to allow them to participate effectively in the creation and growth of high impact pharmaceutical business ventures. The development of this course is in direct response to the demands of industry and its professionals will be highly competitive in the global jobs market.

Certified ModulesModule 1 : Process Engineering in the pharmaceutical industry: An Introduction

Module 2 : Regulatory aspects (India & International): FDA regulations and ICH guidelines, safety aspects, Policy, Legal and statutory framework on industrial safety and health.

Module 3 : Technology Transfer by Process Engineer in pharmaceutical Industry and Various Functions of departments of industry

Module 4 : Stoichiometry & the Role of Chemical Engineering in Pharmaceutical API Process R&D.

Module 5 : Industrial Processes for Reactions, Reactor types & Design with accessories.

Module 6 : Heat and mass Transfer Operations

Module 7 : Process Engineering Package/Docket containing format of Product mapping, physical properties, Utility and its calculation with Variable overheads, Material & energy balance with recycle, PFD, BFD, P & ID, Equipment layout. Materials, Material of construction, Application of codes & standards.

Module 8 : Fluid handling - Fluid flow, Line sizing, Pressure drop calculation, Pipe network analysis, Pumps & Compressor, Steam, compressed air, ETP, refrigeration & HVAC system.

Module 9 : Industrial Unit Processes - Air conditioning & Humidification, Various separation process - Distillation, Evaporation, Crystallization, Filtration & Drying.

Module 10 : Particle Size, Reduction and classification, Mixing

Module 11 : Process Engineering role in Clean Room Management, solid dosage formulation, Sterilization and Bio-processing

Module 12 : Pilot Plant - Scale up and HAZOP study

Module 13 : Material packaging and quality principles.

Module 14 : An Introduction to CHEMCAD


EligibilityAll those who have completed their Diploma and Degree B.E/B.Tech in relevant subject such as Chemical engineering, biochemical engineering, mechanical engineering, manufacturing or industrial engineering, production engineering, Petro Chemical engineering, Sugar Engineering, B. Pharma and Post Graduates such as M. Tech & M.Pharma, are eligible to enroll for this course. As this course is truly professional and industry oriented, employed individuals working in any sector (production, processing, quality, Process engineering, technology transfer, Pilot trial, R&D etc.) in any healthcare industry (Food manufacturing, Food Ingredient and Additive processing, Drugs manufacturing , Medical Device, Ayurveda, Pharmaceutical Industry Regulation, Clinical Research, Homeopathic or Ayurveda Medicine Manufacturing, Cosmetic Manufacturing, Biotechnology) can seek benefits of the course.








Registration The registration dates for this bi-annual program run by the institute are updated timely on the webpage. The Training sessions and webinars are scheduled preferably on weekends depending on the availability of visiting faculty. Effective E-learning tools incorporated into the design of the webpage make the course lectures, videos and study material easily accessible. This gives huge window of self-regulated and self-paced performance to the participants.

Examination & Certification All the participants are expected to appear for an online exam and are also obliged to submit assignments after each module. After successful completion, the participants will be awarded Post Graduate Diploma in Pharmaceutical Process Engineering. For all the above mentioned modules elaborate course material, self-assessment assignments and project work details would be providedby the Institute from time to time. Details get updated on the webpage as well.

Future career prospects of Pharmaceutical Process EngineeringPharmaceutical Process Engineering provides a strong focus on problem solving, Technical, conception, design as well as managerial and practical application of knowledge to particular fact scenarios through a number of advice drafting exercises. The Process Engineer professionals will execute the process development experiments and process optimization of API & formulations, Scale-up of API & formulations from lab scale to pilot/commercial scale, execution of submission batches and validation, Preparation & review of batch documents & protocols.

Process Engineering is important in extending benefits of R&D, Production and engineering to the society at a large, especially in developing countries. Technology Transfer is important for commercialization especially, in the case of developing and underdeveloped countries.

Executive Diploma in Pharmaceutical Process EngineeringPharmaceutical Process engineers are involved in the planning, conception, design, construction/Execution, management, operation of research facilities, pilot plant for scale up, manufacturing plants and labeling & packaging processes in the conversion of chemical and biological materials into valuable pharmaceuticals and pharmaceutical therapies. They have to implement FDA regulations, validation assurance, quality control, and maintain Good Manufacturing Practices (GMP) compliant facilities. In addition to the safety of the end product, they have to maintain a level of personal and environmental safety.

The processes that they come up with are used to create products ranging from oil, gas & drugs to food and drink.

This course will provide a thorough understanding of Process engineering in API and in formulation for develop and design new process and modify existing ones in very cost effective way with safety, increase productivity in existing system, engineering calculations for taking decision at spot etc. This course provides professionals with the skills and knowledge to allow them to participate effectively in the creation and growth of high impact pharmaceutical business ventures. The development of this course is in direct response to the demands of industry and its professionals will be highly competitive in the global jobs market.

This short term programme has been designed mainly to provide brief of Pharmaceutical Process Engineering. The programme provides collecting, linking, and manipulating different types of biological information to discover new biological insight. Thus it works as re-fresher course for those already in the industry and an insight or practical guide for those planning to enter into this sector. You can complete this course from your own city.

Certified ModulesModule 1 : Process Engineering in the pharmaceutical industry: An Introduction

Module 2 : Regulatory aspects (India & International): FDA regulations and ICH guidelines, safety aspects, Policy, Legal and statutory framework on industrial safety and health.

Module 3 : Technology Transfer by Process Engineer in pharmaceutical Industry and Various Functions of departments of industry

Module 4 : Stoichiometry & the Role of Chemical Engineering in Pharmaceutical API Process R&D.

Module 5 : Industrial Processes for Reactions, Reactor types & Design with accessories.

Module 6 : Heat and mass Transfer Operations

Module 7 : Process Engineering Package/Docket containing format of Product mapping, physical properties, Utility and its calculation with Variable overheads, Material & energy balance with recycle, PFD, BFD, P & ID, Equipment layout. Materials, Material of construction, Application of codes & standards.

Module 8 : Fluid handling - Fluid flow, Line sizing, Pressure drop calculation, Pipe network analysis, Pumps & Compressor, Steam, compressed air, ETP, refrigeration & HVAC system.

Module 9 : Industrial Unit Processes - Air conditioning & Humidification, Various separation process - Distillation, Evaporation, Crystallization, Filtration & Drying.

Module 10 : Particle Size, Reduction and classification, Mixing

Module 11 : Process Engineering role in Clean Room Management, solid dosage formulation, Sterilization and Bio-processing

Module 12 : Pilot Plant - Scale up and HAZOP study

Module 13 : Material packaging and quality principles.

Module 14 : An Introduction to CHEMCAD


EligibilityAll those who have completed their Diploma and Degree B.E / B.Tech in relevant subject such as Chemical engineering, biochemical engineering, mechanical engineering, manufacturing or industrial engineering, production engineering, Petro Chemical engineering, Sugar Engineering, B. Pharma and Post Graduates such as M. tech & M.Pharma, are eligible to enroll for this course. As this course is truly professional and industry oriented, employed individuals working in any sector (production, processing, quality, Process engineering, technology transfer, Pilot trial, R&D etc.) in any healthcare industry (Food manufacturing, Food Ingredient and Additive processing, Drugs manufacturing , Medical Device, Ayurveda, Pharmaceutical Industry Regulation, Clinical Research, Homeopathic or Ayurveda Medicine Manufacturing, Cosmetic Manufacturing, Biotechnology) can seek benefits of the course.








Registration The registration dates for this bi-annual executive program run by the institute are updated timely on the webpage. The Training sessions and webinars are scheduled preferably on weekends depending on the availability of visiting faculty. Effective E-learning tools incorporated into the design of the webpage make the course lectures, videos and study material easily accessible. This gives huge window of self-regulated and self-paced performance to the participants.

Examination & Certification All the participants are expected to appear for an online exam and are also obliged to submit assignments after each module. After successful completion, the participants will be awarded Executive Diploma in Pharmaceutical Process Engineering. For all the above mentioned modules elaborate course material, self-assessment assignments and project work details would be provided by the Institute from time to time. Details get updated on the webpage as well.

Future career prospects of Pharmaceutical Process EngineeringPharmaceutical Process Engineering provides a strong focus on problem solving, Technical, conception, design as well as managerial and practical application of knowledge to particular fact scenarios through a number of advice drafting exercises. The Process Engineer professionals will execute the process development experiments and process optimization of API & formulations, Scale-up of API & formulations from lab scale to pilot/commercial scale, execution of submission batches and validation, Preparation & review of batch documents & protocols.

Process Engineering is important in extending benefits of R&D, Production and engineering to the society at a large, especially in developing countries. Technology Transfer is important for commercialization especially, in the case of developing and underdeveloped countries.

Post Graduate Diploma in Pharmaceutical Technology Transfer Technology transfer (TT) includes knowledge transfer, science and risk-based principles including ICH Q8, Q9, Q10, Q11 and efficient processes to meet evolving business needs. Appropriate technology transfer is both integral and critical to drug discovery and development for new medicinal products. It is also important to upgrade drug quality designed during research and development and to finalize product during manufacturing as well as to assure stable quality. This course will provide a thorough understanding of the technology transfer of analytical methods, quality control standards, packaging components, operations and various pharmaceutical dosage forms from R&D to manufacturing. It is designed to provide an understanding of the issues affecting the transfer within and outside a company.

Certified ModulesModule 1 : Introduction to Technology TransferModule 2 : Technology Transfer in Contract Research and Manufacturing Services (CRAMS)Module 3 : Technology Identification & AssessmentModule 4 : Regulatory aspects (India & International): FDA regulations and ICH guidelinesModule 5 : Intellectual Property RightsModule 6 : Customer Relations and Vendor managementModule 7 : Technology valuation, deal making & new product implementationModule 8 : Pharmaceutical Process EngineeringModule 9 : R & D trials and Spin-out DevelopmentModule 10 : Pilot plant-Scale up & Hazop studiesModule 11 : Validation, Commercial plant trials & various functions of departmentsModule 12 : Materials ManagementModule 13 : Technology Transfer Case Studies

EligibilityAll those who have completed their Graduation are eligible to enroll for the course. As this course is truly professional and industry oriented, individuals having experience in any sector (production, processing, quality, trial, R&D etc.) in the Pharma, food and healthcare industry (Drugs manufacturing , Medical Device, Ayurvedic, Pharmaceutical Industry Regulation, Clinical Research, Homeopathic or Ayurvedic Medicine Manufacturing, Cosmetic Manufacturing, Food manufacturing, Food Ingredient and Additive processing, Biotechnology) can also seek benefits of the course.









Examination & Certification All the participants are expected to appear for an online exam and are also obliged to submit assignments after each module. After successful completion, the participants will be awarded Post Graduate Diploma in Pharmaceutical Technology Transfer. For all the above mentioned modules elaborate course material, self-assessment assignments and project work details would be provided by the Institute from time to time. Details get updated on the webpage as well.

Future career prospects of Pharmaceutical Technology TransferPharmaceutical Technology transfer provides a strong focus on problem solving, as well as technical and practical application of knowledge to particular fact scenarios through a number of advice drafting exercises. The Technology Transfer professionals will execute the process development experiments and process optimization of API & formulations, Scale-up of API & formulations from lab scale to pilot/commercial scale, execution of submission batches and validation, Preparation & review of batch documents & protocols.

Technology Transfer is important in extending benefits of R&D to the society at a large, especially in developing countries. Technology Transfer is important for commercialization especially, in the case of developing and underdeveloped countries.

Executive Diploma in Pharmaceutical Technology TransferThis short term programme has been designed mainly to provide brief of Pharmaceutical Technology Transfer. Technology transfer is both integral and critical to the drug discovery and development process for new medicinal products. The decision to transfer products between manufacturing sites is frequently driven by economics. Key stages of the process include data collection, data review, and regulatory impact with particular emphasis on any change approvals, analytical validation, pilot or full-scale process batch, stability. You can complete this course from your own city.

Certified ModulesModule 1 : Introduction to Technology TransferModule 2 : Technology Transfer in Contract Research and Manufacturing Services (CRAMS)Module 3 : Technology Identification & AssessmentModule 4 : Regulatory aspects (India & International): FDA regulations and ICH guidelinesModule 5 : Intellectual Property RightsModule 6 : Customer Relations and Vendor managementModule 7 : Technology valuation, deal making & new product implementationModule 8 : Pharmaceutical Process EngineeringModule 9 : R & D trials and Spin-out DevelopmentModule 10 : Pilot plant-Scale up & Hazop studiesModule 11 : Validation, Commercial plant trials & various functions of departmentsModule 12 : Materials ManagementModule 13 : Technology Transfer Case Studies

Eligibility All those working in the Pharmaceutical Industry or any sector of Healthcare industry or any other industry type (India or abroad) can apply for this short term programme. Life Science Graduate/ diploma holders are eligible for the course. Working professionals of any of the following industry types; Drugs manufacturing , Medical Device, Ayurveda, Pharmaceutical Industry Regulation, Clinical Research, Homeopathic or Ayurveda Medicine Manufacturing, Cosmetic Manufacturing, Food manufacturing, Food Ingredient and Additive processing, Biotechnology or any related industry are highly encouraged to apply for the programme.





Assessment and evaluation for all the programme modules in order to enhance the levels of competencies and skills of the participants leading towards the objective of application in the job.




Examination & CertificationAll the participants are expected to appear for an online exam and are also obliged to submit assignments after each module. After successful completion, the participants will be awarded Executive Diploma in Pharmaceutical Technology Transfer. For all the above mentioned modules elaborate course material, self-assessment assignments and project work details would be provided by the Institute from time to time. Details get updated on the webpage as well.

Future career prospects of Pharmaceutical Technology TransferPharmaceutical Technology transfer provides a strong focus on problem solving, as well as technical and practical application of knowledge to particular fact scenarios through a number of advice drafting exercises. The Technology Transfer professionals will execute the process development experiments and process optimization of API & formulations, Scale-up of API & formulations from lab scale to pilot/commercial scale, execution of submission batches and validation, Preparation & review of batch documents & protocols.

Technology Transfer is important in extending benefits of R&D to the society at a large, especially in developing countries. Technology Transfer is important for commercialization especially, in the case of developing and underdeveloped countries.

For further enquiries:Write to: [email protected] OF GOOD MANUFACTURING PRACTICES INDIAIGMPI, H-119, H Block Sector-63,Noida-201 307,Delhi National Capital Region (NCR), India Phone: +91 8130924488, +91 8587838177, +91 120-4375280, +91 120-2427175

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IGMPI, H-119, H Block, Sector-63, Noida-201 307, Delhi National Capital Region (NCR), India Phone: +91 8130924488, +91 8587838177, +91 120-4375280, 0120-2427175E mail: [email protected]

PROSPECTUS - igmpiindia · PROSPECTUS DRUG DISCOVERY AND DEVELOPMENT PHARMACEUTICAL CHEMISTRY ......

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