Instrumental Methods of Classic Reissue Chemical Analysis ... · Modern Methods of Pharmaceutical...
Transcript of Instrumental Methods of Classic Reissue Chemical Analysis ... · Modern Methods of Pharmaceutical...
Pharmaceutical Analysis / Regulatory Affairs / Pharmaceutical Management
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Introduction to Instrumental Analysis, 2nd Ed.Robert D. Braun
Contents: 1. Introduction to Chemical Instrumental Analysis, 2. Simple DC and AC Electric Circuits, 3. Electronic Circuits,4. Operational Amplifiers, Logic Devices, and Computers, 5. Introduction to Spectral Methods of Analysis, 6. Atomic AbsorptionSpectrophotometry, 7. Flame Emission and Atomic Emission, 8. Atomic Fluorescence, Resonant Ionization, and Laser-EnhancedIonization, 9. Ultraviolet-Visible Spectroscopy of Polyatomic Species, 10. Chemiluminescence and Electrochemiluminescence,11. Fluorescence and Phosphorescence, 12. Infrared Spectrophotometry,13. Photoacoustic Spectroscopy, 14. RadiativeScattering, 15. Refractometry 16. Nuclear Magnetic Resonance Spectroscopy, 17. Electron Spin Resonance Spectrometry,18. X-Ray Methods, 19. Electron Spectroscopy, 20. Radiochemical Methods, 21. Mass Spectrometry, 22. Potentiometry,23. Nonpotentiometric Electroanalysis, 24. Introduction to Chromatography, 25. Liquid Chromatography, 26. Gas Chromatography,27. Thermal Analysis, 28. Automated Analysis
2012 978-93-81075-92-0 1096 pp PB Rs. 995.00
Basics of Drug AnalysisG. Vidya Sagar
Contents: Introduction to Pharmaceutical Analysis 1. Quality Assurance 2. Fundamental Concepts in Volumetric Analysis3. Acidimetry and Alkalimetry 4. Gravimetric Analysis 5. Non-aqueous Titrations 6. Complexometric Titrations 7. DiazotisationTitrations (Sodium Nitrite Titrations) 8. Oxidation–reduction titrations 9. Precipitation Titrations 10. Functional Group Analysis11. Polarography 12. Electro-Analytical Methods or Electro-Chemical methods of Analysis 13. Potentiometry or pH metry14. Amperometric Titrations 15. Solvent Extraction 16. Kjeldahl Method 17. Karl Fischer Titration 18. Oxygen Flask CombustionMethod 19. Errors and Statistics 20. Miscellaneous Methods 21. Gasometry 22. Safety Measures, Prevention and First-Aid inLaboratory 23. Calibration of Volumetric Glassware 24. Radioimmunoassay 25. Polarimetry 26. Refractometry
2009 978-81-88449-67-9 484 pages PB * Rs. 450.00
Instrumental Methods of Drug AnalysisG. Viday Sagar
Contents : 1. Chromatography 2. Column Chromatography 3. Thin Layer Chromatography 4. Paper Chromatography 5. IonExchange Chromatography 6. Gas Chromatography 7. High Performance Liquid Chromatography 8. High Performance ThinLayer Chromatography 9. Introduction to Spectroscopy 10. UV & Visible Spectroscopy 11. Flourimetry 12. Nephelometry andTurbidimetry 13. Atomic Absorption Spectroscopy 14. Flame Photometry 15. Mass Spectroscopy 16. Infrared Spectroscopy17. Nuclear Magnetic Reasonanace Spectroscopy 18. Water Analysis 19. Validation 20. X-ray Spectroscopy
2009 978-81-88449-73-3 546 pages PB Rs. 495.00
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Instrumental Methods ofChemical Analysis, 5th Ed.
Galen W. EwingContents: 1. Introduction, 2. Introduction to Optical Methods, 3. The Absorption of Radiation: Ultraviolet and visible, 4. TheAbsorption of Radiation: Infrared, 5. Atomic Absorption, 6.Molecular Luminescence: Fluorimetry, Phosphorimetry, and RamanSpectroscopy, 7. Photo acoustic Spectroscopy, 8.The Scattering of Radiation, 9. Atomic Emission Spectroscopy, 10. Polarimetry,Optical Rotatory Dispersion, and circular Dichroism, 11. X-Ray Methods, 12. Electron and Ion Spectroscopy, 13. MagneticResonance Spectroscopy,14. Introduction to Electrochemical Methods, 15. Potentiometry, 16. Voltammetry, Polarography, andRelated Methods, 17. Electrodesposition and Coulometry, 18. Conductimetry, 19. Introduction to Chromatography, 20.Gas
Chromatography, 21. Liquid Chromatography, 22.Mass Spectrometry, 23. Thermometric Methods, 24. Nuclear Methods, 25. AutomaticAnalyzers, 26. General Considerations in Analysis, 27. Electronic Circuitry for Analytical Instruments, 28. Computers in Analytical Instrumentation
2013 9781259097072 538 pp PB Rs. 995.00
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Classic Reissue
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Ultraviolet-Visible Spectrophotometry in Pharmaceutical AnalysisSándor Görög
Contents: 1. Introduction 2. The Measurement of Light Absorption (and Reflection) 3. Qualitative Analysis: RelationshipBetween the Structure and Spectra of Pharmaceutical Compounds 4. Quantitative Analysis on the Basis of Natural LightAbsorption 5. Combination of Spectrophotometric Methods with Chromatographic Techniques 6. Spectrophotometric MethodsBased on Chemical Reactions 7. Chemical and Spectroscopic Characterization of Derivatization Reactions 8. DifferenceSpectrophotometry 9. Spectrophotometric Determination of Pharmaceuticals in Various Matrices 10. Spectrophotometric Analysisof Some Important Groups of Drug Compounds.
2011 978-93-81075-31-9 391 pages HB Rs. 1495.00
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2 Phone : 040-23445688 Fax: 91+40-23445611 e-mail: [email protected] website: www.bspublications.net/www.pharmamedpress.comPrices are subject to change without prior notice
Pharmaceutical Analysis / Regulatory Affairs / Pharmaceutical Management
A Textbook of Analytical ChemistryY. Anjaneyulu, K. Chandrasekhar and Valli Manickam
Contents: 1. Introduction to Analytical Chemistry 2. Statistical Treatment of Analytical Data 3. Quantitative Method of Analysis4. Gravimetric Analysis 5. Introduction to Volumetric Analysis 6. Acid-Base Titrations 7. Redox Titrations 8. ComplexometricTitrations 9. Chromatography 10. Paper Chromatography 11. Thin Layer Chromatography 12. Gas Chromatography (GC) 13.High Performance Liquid Chromatography 14. Column Chromatography 15. Ion Exchange Chromatography 16. Gel PermeationChromatography (GPC) 17. Spectroscopy 18. UV Visible Spectroscopy 19. Turbidimetry and Nephelometry 20. MolecularFluorescence & Phosphorescence and Chemiluminescence Spectrometry 21. Infra-Red Spectroscopy 22. Raman Spectroscopy23. Atomic Emission, Fluorescence and Absorption Spectroscopy 24. Flame Photometry 25. Inductively Coupled Plasma-Optical Emission Spectrometry (ICP–OES) 26. Inductively Coupled Plasma–Mass Spectrometry (ICP-MS) 27. Mass Spectroscopy 28. Photoacousticspectroscopy 29. X-Ray Absorption, diffraction and Fluorescence Spectroscopy 30. Nuclear Magnetic Resonance Spectroscopy 31. Electron SpinResonance Spectroscopy 32. Thermal Analysis 33. Electro Analytical Chemistry 34. Potentiometry 35. Conductometry 36. Electrogravimetry 37.Coulometric methods of analysis 38. Voltammetry
2009 81-88449-19-9 892 pages PB Rs. 595.00
Modern Methods of Pharmaceutical Analysis, 2nd Ed. 2 Vol. SetRoger E. Schirmer
During the development of a new drug product, detailed chemical studies must be made of raw materials, syntheticintermediates, the drug substance itself, and the final formulated product. These studies must identify types and levels ofimpurities, degradation products, degradation rates, and analytical methods suitable for monitoring these factors. Theinformation resulting from these studies is used to identify potential sources of safety problems in the product, to meet therequirements of foreign and domestic regulatory agencies, and as a basis for establishing quality control procedures andspecifications for the product. The analytical effort required to provide this information can be divided into a number of tasks.The requirements for specificity, precision, accuracy, and the degree of complexity acceptable in the analytical procedurevary considerably from task to task and therefore require a variety of analytical techniques to satisfy them. The set ofanalytical procedures developed to control the quality of the final marketed product must include both qualitative andquantitative methods in order to assure the identity and purity of the product. Several categories of tests are usually included
in a product specification.Contents: Volume I: 1. Separation of Drugs from Excipients 2. UV and Visible Absorption Techniques 3. IR Methods of Analysis 4. Near InfraredMethods of Analysis 5. Fluorometric Analysis 6. Optical Rotation 7. Nuclear Magnetic Resonance Spectroscopy 8. Thermal Analysis 9. PhaseSolubility Analysis Volume II: 1. Polarography 2. Coulometry 3. Gas-Liquid Chromatography 4. High-Performance Liquid Chromatography 5. TheDetermination of Isomeric Purity
Rpt. 2010 9781405146531 Vol. I: 400 pages Vol. II: 456 pages HB Set price Rs. 3250.00
Identification and Determination of Impurities in DrugsS. Gorog
Contents: 1. Various aspects of the estimation of impurities in drugs, 2. Identification, structure elucidation and determinationof related organic impurities, 3. Identification and determination of residual solvents, 4. Identification, semiquantitative andquatitative determination of inorganic impurities, 5. Degraduation products as impurities, 6. Determination of enantiomericimpurities, 7. Estimation of polymorphic modifications as impurities in drugs, 8. Microbiological examination of non-sterile drugsand raw materials, 9. Selected examples (impurity profiling of some groups of drugs)
Rpt. 2012 9789381269626 748 pp HB Rs. 2195.00
Analytical InstrumentationBela G. Liptak
Contents: 1. Analyzer Application and Selection 2. Analyzer Sampling-Process Samples, 3. Analyzer Sampling-StackParticulates, 4. Air Quality Monitoring, 5. Biometers, 6. Biochemical Oxygen Demand (BOD), Chemical Oxygen Demand (COD),Total Oxygen Demand (TOD), 7. Calorimeters, 8. Carbon Dioxide, 9. Carbon Monoxide 10. Chlorine 11. Chromatographs-Gas,12. Chromatographs-Liquid, 13. Coal Analyzers, 14. Colorimeters, 15. Combustibles 16. Conductivity Analyzers, 17. ConsistencyAnalyzers, 18. Corrosion Monitoring, 19. Differential Vapor Pressure Sensor, 20. Dioxin Analysis, 21. Elemental Monitors,22. Fiber-Optic Probes, 23. Fluoride Analyzers, 24. Hydrocarbon Analyzers, 25. Hydrogen Sulfide, 26. Infrared Analyzers,27. Non-Selective Electrodes, 28. Mass Spectrometers, 29. Mercury in Air, 30. Mercury in water, 31. Moisture in Air: Humidity
and Dew point, 32. Moisture in Gases and Liquids, 33. Moisture in Solids, 34. Molecular Weight, 35. Nitrate, Ammonia, and total Nitrogen, 36. Nitrogenoxide Analyzers, 37. Odor Detection, 38. Oil in or on Water 39. Oxidation-Reduction Potential (ORP), 40. Oxygen in gases, 41. Oxygen in liquids(dissolved oxygen), 42. Ozone in Gas, 43. Ozone in water, 44. Particulates, Opacity, Dust, and Smoke, 45. Particle size and Distribution Monitors,46. pH measurement 47. Phosphorus Analyzer, 48. Physical properties analyzers-ASTM methods, 49. Refractometers 50. Streaming current onparticle charge analyzer, 51. Sulfur-in-oil Analyzers, 52. Sulfur oxide Analyzers, 53. Thermal Conductivity detectors,54. Total Carbon Analyzers,55. Toxic Gas Monitoring, 56. Turbudity, Sludge, and Suspended solids, 57. Ultraviolet and Visible Analysis 58. Viscometers-Application andSelection, 59. Viscometers-Laboratory, 60. Viscometers-Industrial, 61. Voltametric, Amperometric, and other Electrochemical Analyzers,62. Water Quality Monitoring, 63. Wet-Chemistry and Analyzers
Rpt.2012 0-80-19839-75 471 pp PB Rs. 1395.00 Vis
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Pharmaceutical Analysis / Regulatory Affairs / Pharmaceutical Management
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Practical Manual of Analytical ChemistryNeelam Singla, Navneet Kaur and Kanchan Kohli
2012 978-93-81075-63-0 166 pp PB Rs. 100.00
Liquid Chromatography-Mass Spectrometry, 3rd Ed.Wilfried M.A. Niessen
Contents: INTRODUCTION: 1. Liquid Chroma-tography and Sample Pretreatment 2. Mass Spectrometry TECHNOLOGY3. Strategies in LC–MS Interfacing 4. History of LC–MS Interfaces 5. Interfaces for Atmospheric-Pressure Ionization6. Atmospheric-Pressure Ionization APPLICA-TIONS: SMALL MOLECULES 7. LC–MS Analysis of Pesticides 8. EnvironmentalApplications of LC–MS 9. LC–MS in Drug Discovery and Development 10. LC–MS in Drug Metabolism 11. Quantitative BioanalysisUsing LC–MS 12. Clinical Applications of LC–MS 13. LC–MS Analysis of Steroids 14. LC–MS in Food Safety Analysis 15. LC–MS Analysis of Plant Phenols APPLICATIONS: BIOMOLECULES 16. LC–MS analysis of Proteins 17. LC–MS analysis ofPeptides / Enabling Technology 18. LC–MS in Proteomics 19. LC–MS for Identification of Post-Translational Modifications20. LC–MS Analysis of Oligosaccharides 21. LC–MS Analysis of Lipids and Phospholipids 22. LC–MS Analysis of Nucleic Acids
Rpt. 2009 978-082474-082-5 632 pp PB Rs. 995.00
Solvent RecoveryHandbook, 2nd Ed.
Ian M Smallwood
Rpt. 2005 978-1-40514-653-1432 pages HB Rs. 1750.00
Laboratory Auditing ForQuality and RegulatoryCompliance
Donald Singer, Raluca-Ioana Stefan,Jacobus van Staden
Rpt. 2007 9781574445701496 pages HB Rs. 2750.00
Pharmaceutical Plant AdministrationManohar A. Potdar
Contents: PART – I Basic Principles of Management 1. Introduction 2. Planning 3. Organising 4. Staffing 5. Leading6. Controlling PART – II Practice of Pharmaceutical Plant Administration 1. Introduction 2. General Administration3. Production 4. Production Planning and Control 5. Quality Management 6. Warehousing 7. Engineering 8. Personnel and HRD
2013 978-81-7800-303-0 323 pp PB Rs. 395.00
Pharmaceutical Management
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Steroid Analysis in the Pharmaceutical Industry :Hormonal Steroids, Sterols, Vitamins D, Cardiac Glycosides
S. GÖRÖG
Contents: 1. Introduction 2. Methods used in steroid analysis 3. Structural elucidation of steroids 4. Analytical control of theproduction of steroids 5. Analytical control of steroid formulation 6. Determinations of steroids in biological media
Rpt. 2007 81-88449-24-5 398 pages HB Rs. 950.00
Pharmacy AdministrationG. Vidya Sagar
Contents: 1. Introduction to Business 2. Manufacturing Management 3. Social Use of Drugs, Drug Addiction 4. Organisationof Distribution and Marketing 5. Pharmaceutical Industry 6. Insurance 7. Governance in Pharmacy 8. Drug Store Principles andManagement
2010 978-81-7800-255-2 436 pages PB Rs. 250.00
Mass Spectroscopy : A TextbookJurgen H. Gross
Contents: 1. Introduction 2. Gas phase ion chemistry 3. Isotopes 4. Instrumentation 5. Electron Ionization 6. Fragmentation oforganic lons and Interpretation of EI mass spectra 7. Chemical ionization 8. Field ionization and Field Desorption 9. Fast atombombardment 10. Matrix assisted laser desorption / ionization 11. Electrospray ionization 12. Hyphenated methods
Rpt. 2007 978-81-812868-57 536 pages HB Rs. 1595.00
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Pharmaceutical Analysis / Regulatory Affairs / Pharmaceutical Management
Pharmaceutical Facilities:Design, Layouts and Validation, 2nd Ed.
Manohar A. PotdarContents: PART-I 1. Regulatory Requirements for Pharmaceutical Plants 2. Project Management 3. Pharmaceutical ValidationPART-II 4. Pharmaceutical Facilities Design 5. Support Services Department 6. Support Services for Plants
2014 978-81-7800-328-3 276 pages HB Rs. 1295.00
Pharmaceutical Management
Compete or Forfeit !CompetitiveStrategies forPharmaceuticalIndustry
Subba Rao Chaganti
2007 81-88449-26-1400 pages HB Rs. 695.00
Pharmaceutical Industrial ManagementG. Vidya Sagar
Contents : 1. Management 2. Principles of Management 3. Administrative Management 4. Production Management5. Materials Management Control 5-A Materials Management 5-B Inventory Control 6. Personnel Management 7. PharmaceuticalMarketing 8. Channels of Distribution 9. Salesmanship 10. Marketing Research 11. Personnel Management Functions12. Accounting and its Principles 13. Recording of the Business Transactions 14. Trial Balance and Errors 15. FinancialStatements 16. Bank Reconciliation Statement 17. Bills of Exchange 18. Treatment of Cheques 19. Economics 20. Trade21. Insurance 22. Labour Welfare
2009 978-81-88449-12-5 365 pages PB * Rs. 325.00
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Pharmacoethics: A Problem-based ApproachGettman David A.
Contents: 1. Professional Responsibility 2. Patients’ Rights 3. Privacyand Confidentiality 4. Ethics Committees 5. Patient Privacy 6. Truth Telling7. Reproductive Ethics 8. Genetic Screening 9. Seriously Ill Neonates10. Distributive Justice 11. Unethical Experimentation 12. ResearchPrinciples 13. Scientific Integrity 14. Research on Human Subjects15. Research/Testing on Animals 16. Intellectual Property 17. GermlineTherapy 18. Medical Surveillance
Rpt. 2010 978-1587160356 472 pages PB Rs. 995.00
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Textbook of Forensic Pharmacy, 2nd Ed.C.K. Kokate and S.B. Gokhale
Contents: 1. General Introduction, 2. History of Drug Legislation and Pharmacy Profession in India, 3. Pharmaceutical Ethics,4. The Pharmacy Act, 1948, 5.The All India Council for Technical Education Act, 1987, 6. The University Grants Commission(U.G.C.) Act, 1956, 7. The Drugs and Magic Remedies (Objectionable Advertisements) Act, 1954 and Rules, 1955, 8. TheDrugs and Cosmetics Act, 1940 and Rules, 1945, 9. Good Clinical Practice (GCP),10. The Narcotic Drugs and PsychotropicSubstances Act, 1985 and Rules, 1985, 11. Medicinal and Toilet Preparations (Excise Duties) Act, 1955 and Rules, 1956,12. The Industries (Development and Regulations) Act, 1952,13. Medical Termination of Pregnancy Act, 1971 & Rules, 2003,14.Essential Commodities Act, 1955, 15. Insecticides Act, 1968, 16. The Consumer Protection Act, 1986, 17. Poisons Act,1919, 18. Shops and Establishments Act, 19. Prevention of Cruelty to Animals Act, 1960, 20.The Prevention of Food Adulteration
Act, 1954 and Rules, 1955, 21.National Pharmaceutical Pricing Authority (NPPA), 22. National Blood Policy, 23. Pharmaceutical Policy-2002, 24. TheDrugs (Price Control) Order(DPCO), 1995, 25. WTO, GATS and The Indian Patents Act, 1970 with Amendments, 26. Good Laboratory Practice(GLP), 27. Adverse Drug Reactions (ADRs), 28. List of Prohibited Drugs in India
2012 230 pp 978-93-81075-99-9 PB * Rs. 250.00
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Concepts of Quality Management in Pharmaceutical IndustryManohar A. Potdar
Contents: 1. Understanding Quality, 2. Companywide Quality Assessment, 3. Quality Organisation, 4. Quality Culture,5. Strategic Quality Management, 6. Designing for Quality, 7. Quality Planning, 8. Quality Control, 9. Quality Assurance andAudits, 10. Quality Improvement, 11. Quality Manufacturing, 12. Acceptance Sampling, Inspection, Test and Measurement,13. Statistical Process Control
2014 978-93-83635-09-2 265 pages HB Rs. 1495.00
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Quantitative Drug Design: A Critical Introduction, 2nd Ed.Martin Yvonne C
Contents: 1. Overview of Quantitative Drug Design 2. Non-Covalent Intermolecular Interactions of Importance to BiologicalSystems 3. Traditional QSAR Substituent Effects on Physical Properties Calculated from 2D Structures of molecules 4. QSARMolecular Properties Calculated from 3D Structures of Molecules 5. Biological Data 6. The Form of the Equation that RelatePotency and Physical Properties 7. Principles of Multivariate Statistical Analysis 8. Strategy in the Statistical Evaluation of a RealData Set 9. A Detailed Example of Calculations of a 2D and a 3D QSAR 10. Other Mathematical Methods of use in QuantitativeStructure Activity Studies 11. Selection of Compounds for Synthesis to Follow Up a Lead: How to Start and When to Stop12. Case Studies in QSAR 13. Computer Recognition or Design of New Molecules
Rpt. 2013 978-1-4200-7099-6 392 pages PB Rs. 1095.00
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Pharmaceutical Analysis / Regulatory Affairs / Pharmaceutical Management
5Phone : 040-23445688 Fax: 91+40-23445611 e-mail: [email protected] website: www.bspublications.net/www.pharmamedpress.comPrices are subject to change without prior notice
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Quality Assurance and Quality Management inPharmaceutical Industry
Y. Anjaneyulu, R. MarayyaContents : 1. Introduction 2. Elements, Requirements and Interpretation of ISO 9001 : 2000 Quality Management System3. Good Laboratory Practice (GLP) 4. Methods of Analytical Quality Assurance (AQA) 5. Interpretation of Good ManufacturingPractice-Guide for Active Pharmaceutical Ingredients 6. Statistical Quality Control 7. Quality Audit
2009 978-81-88449-80-6 362 pages PB Rs. 395.00
cGMPCurrent Good Manufacturing Practices for Pharmaceuticals
Manohar A. PotdarContents : 1. Personnel 2. Surroundings, Buildings and Facilities 3. Equipment 4. Materials Management 5. Quality Management6. Manufacturing Operations and Control 7. Documentation and Records 8. Pharmaceutical Validation 9. Out Sourcing 10. PostOperational Activities 11. Sterile Pharmaceutical Products 12. Site and Plant Security 13. Safety and Environmental Protection14.Good Pharmaceutical Wholesaling Practices 15. Pharmaceutical Audit
2009 978-81-88449-78-4 798 pages PB * Rs. 750.00
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Pharmaceutical Quality Assurance and ManagementK. P. Bhusari, U. D. Shivhare, D. C. Goupale
Contents: Part I: Guidelines in Pharmaceuticals 1. Introduction to Clinical Pharmacy 2. Audit Guide Line Formats forPharmaceutical Excipients 3. Good Laboratory Practices 4. Good Clinical Practice Guidelines 5. Hazard and Risk Analysis inPharmaceutical Products 6. Validation Protocols 7. Pharmaceutical Inspections Part II: Regulations in Pharmaceuticals8. The Consumer Protection Act, 1986 9. The Environment (Protection) Act, 1986 10. Scale up and Post Approval ChangesPart III: Quality Management in Pharmaceuticals 11. Quality Management System for API’s (GMP and ISO) 12. ProcessAnalytical Technology 13. Quality Risk Management 14. Quality Management of Cosmetics
2013 978-81-7800-276-7 562 pages PB Rs. 495.00
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IPR Handbook for Pharma Students and ResearchersParikshit Bansal
Contents : 1. What are IPRs? 2. How are IPRs practically useful for pharma students and researchers? 3. How can I file apatent? 4. How should I commercialize my patent? 5. How can I integrate IPRs into my research work? 6. Why are ethicsimportant in the study of IPRs? 7. What are the important treaties and international agreements I should be aware of as a Pharmastudent? 8 What are the career options for me in the area of IPRs? 9. How can I improve my qualifications in the area of IPRs?
2009 81-88449-33-4 218 pages PB * Rs. 350.00
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Environmental Management: A Primer for Industries I. V. Murali Krishna and Valli ManickamContents: 1. Introduction 2. Internal Environmental Laws, 3. National Environmental Laws, 4. Life Cycle Assessment,5. Environmental Impact Assessment, 6. Environmental Audit, 7. Environmental Accounting, 8. Environmental Risk Assessment,9. Energy Management and Audit 10. ISO 9000, 14000 Series and OHSAS 18001, 11. Water Treatment Technologies,12. Waterwater Treatment Technologies, 13. Industrial Wastewater Treatment Technologies, 14. Air Pollution and ControlTechnologies, 15. Noise Pollution, 16. Solid Waste Management 17. Hazardous Waste Management, 18. Methods of Analysisfor Water, WasteWater, Soil and Air
2014 978-93-83635-28-3 588 pages HB Rs. 2495.00
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Safety andHealthinIndustry:A Handbook
A. M. Sarma
2009 375 pp978-81-7800-183-8BSPBSP HB Rs. 1495.00
Quality : A Critical Introduction, 3rd Ed.Beckfordg John.L.W
Contents: 1. The Quality Imperative 2. Quality: A Strategic Decision? 3. Barriersto Quality 4. The Emergence of Management Part Two: The Quality Gurus UserGuide 5. Philip B. Crosby 6. W. Edwards Deming 7. Armand V. Feigenbaum8. Kaoru Ishikawa 9. Joseph M. Juran 10. John S. Oakland 11. Taiichi Ohno12. Shigeo Shingo 13. Genichi Taguchi Part Three: Contemporary Thinking UserGuide 14. Contingency Theory 15. Organisations as Systems 16. OrganisationalCybernetics 17. Soft Systems Thinking 18. Critical Systems Thinking 19. BusinessProcess Re-engineering 20. Organisational Learning 21. Systemic Quality
Management Part Four: Methods, Tools & Techniques User Guide 22. SB Foods: A Quality Problem?23. First Intervention 24. Second Intervention 25. Final Intervention
2011 328 pp 978-0-41599-635-8 BSPT&F PB Rs. 595.00
21st Century Pharmaceutical DevelopmentPeter Blaisdell
Contents: 1. Financing Strategies for small Drug Developers, 2. Managing Basic Research in the Twenty-FirstCentury, 3. Protecting Intellectual Property in the New Millennium, 4. The Marketing of Pharmaceutical Products, 5. RegulatoryAffairs in the Twenty-First Century, 6. Advances in Preclinical Toxicology Studies for Pharmaceutics, 7. Drug Product FormulationDevelopment, 8. Twenty-First Century Manufacturing, 9. The Art (and Science) of Developing a Clinical Strategy, 10. The Roleof Statistics in Drug Development, 11. Project Management in Drug Development, 12. Outsourcing in PharmaceuticalDevelopment, 13. Diagnostics, 14. Medical Devices
Rpt. 2004 1-57491-102-3 388 pages HB Rs. 4495.00
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International Journal ofDrug Design and DiscoveryAn International Quarterly Research Journal of Drug Design and Discovery
Chief Editor : D. Sriram, BITS-Pilani Hyderabad Campus.
Commissioning Editor: P. Yogeeswari, BITS-Pilani Hyderabad Campus.
Volume 5, 2014 (January, April, July, October), ISSN: 0975-8275
(*Subscription should be paid in advance) Bank DD / Local Cheque should be drawn in favour of PharPharPharPharPharma Book Syndicama Book Syndicama Book Syndicama Book Syndicama Book Syndicatetetetete
Subscription* DetailsOne Year (4 issues: January-December) Rs. 5000.00
YOU CAN SEND YOUR SUBMISSION OF PAPER / ARTICLE REQUEST ATe-mail: [email protected] / [email protected]
For more details please visit us at : www.ijdddonline.com
We have instituted “Best Research Paper Award” to recognize outstanding achievement inpharmaceutical science as demonstrated by the author in quality and originally of the
manuscript published in the International Journal.
BESTRESEARCH
PAPER AWARD **
Experimental Pharmaceutical AnalysisNavapreet Dhillon
Contents: 1. Acid Base Titrations 2. Oxidation Reduction Titrations 3. Precipitation Titrations 4. Gravimetric Titrations 5. Non-aqueous Titrations6. Complexometric Titrations 7. Kjeldahl Method 8. Karl Fischer Titration 9. Diazotization Titrations 10. Conductometric Titrations 11. Flame Photometry12. Polarimetry 13. Ion-Exchange Chromatography 14. Electrophoresis 15. Thin Layer Chromatography 16. Column Chromatography 17. Colorimetry18. Spectrofluorometry 19. UV/ Visible Spectroscopy 20. Infrared Spectrophotometry
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Handbook of Environmental Laws,Acts, Guidelines, Compliances & Standards, 3rd Ed. 2 Vol. Set
Dr. R. K. TrivedyContents: Volume I: I. Introduction II. Indian Constitution & Environment, Environmental Policy of India & the LegislativeFramework III. Institution Mechanism & Environmental Policy IV. Environmental Clearance & Guidelines for IndustriesV. Environmental Standards VI. Hazardous Wastes VII. Environmental Audit VIII. Water Pollution IX. Air Pollution X. PublicLiability Insurance XI. National Environment Appellate Authority XII. National Environment Tribunal XIII. Indian Forest ServiceXVI. Wildlife Volume II XVII. Animal Welfare XVIII. Environment Protection
2010 978-81-7800-221-7 HB (Set of two volumes) Rs. 4000.00
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