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c gmp (current good manufacturing practices)
A brief presentation on the current good manufacturing practices employed in the manufacture of phar...
Clinical Trials Phases:- 1) Definition 2) Pre-clinical Studies 3) Clinical Phases a) Phase 0 b) Phas...
Clival Database offers unparalleled access to detailed clinical trial records, helping researchers t...
Special emphasis on Q series guidelines
Good Manufacturing Practice is a set of regulations, codes, and guidelines for the manufacture of d...
The ability of a pharmaceutical product to retain its chemical, physical, microbiological and biopha...
pharmacogenomics, pharmacology, and personalized medicine
drug development, IND, withdrawl of IND, exemption, IND review,
B. Pharm. Final Year, Sem-VIII, BP804 ET: PHARMACEUTICAL REGULATORY SCIENCE (Theory). Unit-I Chapter...
Details of animal toxicity and GLP
in this presentation about the dope testing for athletics who do doping and play game and win becau...
impurity and stability studies m pharmacy
This PPT covers the B. Pharm, Pharmaceutical Jurisprudence Unit-I topics with Objectives, Definition...
This involves alternatives methods for the animal testing and their benefits.
About the methods of bracketing and matrixing ICH Q1D guideline
PRECLINICAL TEST
Regulatory affairs
Natural product
Dr. William Kritsonis Public School Law
Pharmaceutical Regulataory Affairs
An IND is a submission to the food and drug administration (FDA) requesting permission to initiate a...
Parenterals: An In-Depth Overview
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