Found 21 presentations matching your search
Submitted during Marketing Management project.
Brand Dossier
Pharmaceutical regulatory affair is the interface between pharmaceutical industry and the regulatory...
Process involved in Generic product development
Technical Dossier filing requirements for Emerging market
Investigational medicinal product dossier (IMPD) and Investigational brochure (IB) in Regulatory aff...
Regulatory Requirements OF REST OF THE WORLD Countries by DIVYA PUSHP
Clinical significance of bioequivalence and biowaivers
Abbreviated New Drug Application (ANDA) Submission: Introduction Basic Generic Drug Requirements Goa...
Pharmacoeconomics is the one of the evolving area in Clinical pharmacy. Let's go through the his...
GCC countries, Drug registration regulations of Saudi Arabia, Medicinal Product Registration proces...
Documentation in Pharmaceutical Industry - master formula record , DMF ( DRUG MASTER FILE )
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Master formula record, DMF (Drug Master File), Distribution records. Generic drugs product developme...
About the submission of IND, NDA and ANDA.
5. Unit-V- Regulatory Concepts. B. Pharm. Final Year, Sem-VIII, BP804 ET: PHARMACEUTICAL REGULATORY ...
Drug safety reporting has a vital role in the pre-approval and post-approval phases. It is essentia...
703834270-David-Strategic-Management-17e-Accessible-PowerPoint-03[1].pptx703834270-David-Strategic-M...
As an example focus case study, we shared our initial Tier-1 assessment results on acrylamide exposu...
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