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www.knbcpharmasolutions.com
NBC Pharma Solutions
Training Duration : 20 Working DaysTheory Hours : 20 HoursTheory with online Practical Hours : 40 HoursMaximum Class Size : 20 Members
Reach us:
KNBC PHARMA SOLUTIONS PVT. LTD.3rd Floor, Plot No. 177, I. D. A. Mallapur
Hyderabad - 500 076, Andhra Pradesh, India.
Reach us:
3rd Floor, Plot No. 177, I. D. A. MallapurHyderabad - 500 076, Andhra Pradesh, India.
KNBC PHARMA SOLUTIONS PVT. LTD.
We are specially designed 100% certified job oriented
"HANDS ON TRAINING" programme for Science
and Pharmacy Graduates and jobseekers on
“PHARMACEUTICAL ANALYSIS TRAINING”. The
course covers various testing procedures adopted in
Pharmaceutical Industries (Bulk Drugs and
Formulations). Practical Training will be provided on
latest Instruments. The training also covers the
Topics on facing Interview, personality development,
Quality Control and Analytical Development. We also
impart training to individuals to suite their needs as
per their requirement.
LC MS/MS Operation, Calibration & Troubleshooting
HPLC Operation, Calibration and Trouble Shooting
GC Operation, Calibration and Trouble Shooting
FTIR Operation, Calibration and Trouble Shooting
Dissolution Tester Operation, Calibration and
Trouble Shooting
Disintegration Tester Operation and Calibration
Volumetric Solutions Preparation and
Standardization
Friability Tester Operation and Calibration
Limit Test Analysis (Sulphates, Chlorides and etc)
TLC Techniques
All types of Instrumental Analysis of Tablets,
Injectables and Bulk drugs
All types of Chemical Analysis of Tablets,
Injectables and Bulk drugs
TRAINING TOPICS
(THEORY WITH PRACTICALS)
TRAINING TOPICS
(THEORY WITH PRACTICALS)
ABOUT USABOUT US
SERVICESSERVICES
KNBC pharma solutions is testing laboratory equipped
with Highly qualified and well experienced scientific team
Strict adherence to its core values of ethics, safety and
reliability in supporting to work for customers. Imparting
best analytical services to various clients who are into
manufacturing of Bulk drugs, Api's, Formulation, research
and development and government agencies.
Analytical Services
Synthetic Services
Auditing Services
Guidelines Followed:
·
· Analytical method validations
· Estimation of Genotoxic impurities
· Answering Rugulatory / Agency queries
· Isolation of process related impurities by
Preparative
· Preparation of Intermediates
· Synthesizing of process related impurities.
· Optimizing the Cost effective Synthetic
schemes
Independent quality assurance team
· Performing Study based audits
· Performing process based audits
· Performing Facility based audits
· Performing quality based audits
Indian pharmacopia(IP)
British pharmacopia (BP)
United states pharmacopia (USP)
Europian pharmacopia (EP)
ICH guidelines
Analytical Method development
·
1. IMPURITY ISOLATION
2. IMPURITY SYNTHESIS
3. CERTIFIED IMPURITY STANDARDS
4. COST EFFECTIVE SCIENTIFIC SOLUTION
5. LYOPHILIZATION SERVICES
6. OTHER USER SPECIFIC SUPPORT
7. STRUCTURE INTERPRETATION
Isolation and purification of impurity from mg to g scale. We have executed most critical isolation and purification project in recent past, e.g isolation of unknown impurity from drug product and APIs and and Structure elucidation.
We have synthesized impurities as on date. We offer custom synthesis of impurity compounds on requests. For a quote on this service please submit the following information:
A) Structure of the impurity. B) Name of the parent compound. C) Required quantity.
All products are supplied with certificates of analysis. Standard certificates contain:
A) Identification by 1H-NMR and Mass spectroscopy. B) Purity test by either HPLC or GC. C) Other test like C13-NMR, TGA, IR & Elemental Analysis will be provide on request.
We are manufacturing impurity in gm level. Our prices are lowest prices in the world.
We are providing this typical service, all kinds of sample which are very sensitive to temperature.We have Virtis 25EL, Capacity of freeze drying is 500 g/day.
We are supporting our client for analytical method development, formulation development, in-vitro-invivo studies, preformation studies, impurity profiling, leaching study, tech-tanfer issues and FDA query response.
Study of spatial heterogeneity of reactants, products, or conditions by using 2-D NMR techniques involving Homonuclear correlation experiments like NOESY, DQF-COSY, TOCSY, ROESY and Heteronuclear correlation experiments like HMQC, HSQC, HMBC.Quantification studies by NMR. MS/MS studies and mass accuracy up to 4th decimal - Q-TOF. For volatile / neutral molecules with less than 500 amu GCMS,
t Screening of Genotoxic Impurities
t Evaluation & Estimation of Genotoxic
Impurities & Method Validation
t Analytical Method Validation of
Pharmacopoeial Methods
t Analytical Method Validation of
Related Substances (Impurity Profile)
t Analytical Method Validation of
Residual solvents in ppm levels
t Analytical Method Validation of Assay
(Chromatographic and potentiometric)
t Analytical Cleaning Method Validation
of Rinsing and Swab method
t Analytical Method Validation of Chiral
Method by HPLC
t Injectables, Syrups, Ointments
t Formulation Tablets, Capsules
t Excipients
t Raw Materials
t Intermediates and In-process
Samples
t Identification by IR, UV, HPLC, GC, MR
t Related Substances by HPLC, GC
t Assay by HPLC, GC, UV, Potentiometer
t Residual Solvents by Headspace
method and Liquid method
t Loss on Drying
t Limit Tests for Metals (As per
Pharmacopoeia method)
t Residue on Ignition Solubility test
t Melting Point and Range
OUR STRENGTHOUR STRENGTH