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this is a detailed study on classification of all kind of antibiotic drugs .... a detailed pharmacol...
here you can learn details about Preclinicals studies, clinical trails and Pharmacovigilances
Safety data generation Pre clinical phase Clinical phase Post approval phase (PMS)
Contents: European Medicines Agency (EMA) IMPD Introduction Contents of IMPD Objectives Scope Intro...
Introduction to pharmacognosy
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ich guidelines for clinical trials, general principles, scientific approach .
This presentation will give you an overview about intellectual property rights of kani tribes and ho...
The differential diagnosis of drug-induced liver disease involves distinguishing it from other liver...
IND
INVESTIGATIONAL NEW DRUG APPLICATION AS PER FEDERAL FOOD DRUG AND COSMETIC ACT
CTD eCTD organization of CTD & eCTD CTD triangle Module 1 to 5
An IND is a submission to the food and drug administration (FDA) requesting permission to initiate a...
COMMON TECHNICAL DOCUMENT , its granularities, benefits, advantages, shortcomings.
Crp
Safety pharmacology is a critical discipline that evaluates the potential adverse effects of new pha...
Preclinical Development, Introduction Definition, Stages of development of a new drug, Objectives of...
The Quick explanation on investigators brochure used in Clinical Trial/Research by the principal inv...
CTD for B. pharmacy And M. pharmacy
Common technical Documents.
The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human ...
COMMON TECHNICAL DOCUMENT
This presentation provides a comprehensive overview of Pharmacology the science of drugs and their ...
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