Found 66 presentations matching your search
What is Lean Authoring? Why Lean Authoring? Advantages of Lean Authoring How to apply Lean Authoring...
Regulatory affairs
ICH GUIDELINES OF EFFICACY AND MULTIDISCIPLINARY
Unit-III, Chapter 1. Registration of Indian Products in Overseas Market. B. Pharm. Final Year, Sem-V...
It's all about the topic of documentation in pharmaceutical industry. In this the specifications...
Abbreviated New Drug Application ANDA ppt by Akanksha puri
COMMON TECHNICAL DOCUMENT , its granularities, benefits, advantages, shortcomings.
- Whilst the realization of the CTD took many years, there is now a common format for the submission...
Providing Submissions in Electronic Format — Post marketing Safety Reports
It is applicable for the Generic drugs
ICH GUIDELINE .M.PHARM , B.PHARM REGULATORY AFFAIRS
Basic information for beginners...
It is unique in bringing together the regulatory authorities and pharmaceutical industry to discuss...
This presentation gives knowledge on ICH and its History, Mission, and overview of ICH Quality, Safe...
This presentation gives a complete brief idea of how FDA regulates the marketing of Generic drugs. A...
GCC countries, Drug registration regulations of Saudi Arabia, Medicinal Product Registration proces...
good
This SlideShare presentation provides a comprehensive exploration of Good Clinical Practice (GCP) as...
LAW
ICH GUIDELINES, ICH, INTERNATIONAL CONFERENCE ON HARMONIZATION, B PHARMA 6TH SEM, PHARMACEUTICAL QUA...
It involves origin, evolution, objectives,
DMF of Japan and Drug Regulatory Approval procedure
REGULATORY AFFAIRS
ICH Guidelines
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