Found 59 presentations matching your search
overview of dossier
Basic information for beginners...
Unit-III, Chapter 1. Registration of Indian Products in Overseas Market. B. Pharm. Final Year, Sem-V...
Abbreviated New Drug Application ANDA ppt by Akanksha puri
It's all about the topic of documentation in pharmaceutical industry. In this the specifications...
DMF of Japan and Drug Regulatory Approval procedure
It is applicable for the Generic drugs
This ppt focuses on the efficacy and multidisciplinary guidelines of ICH guidelines.
- Whilst the realization of the CTD took many years, there is now a common format for the submission...
What is Lean Authoring? Why Lean Authoring? Advantages of Lean Authoring How to apply Lean Authoring...
ICH GUIDELINES OF EFFICACY AND MULTIDISCIPLINARY
This SlideShare presentation provides a comprehensive exploration of Good Clinical Practice (GCP) as...
Technical Dossier filing requirements for Emerging market
LAW
Regulatory Requirements OF REST OF THE WORLD Countries by DIVYA PUSHP
ICH GUIDELINE .M.PHARM , B.PHARM REGULATORY AFFAIRS
It is unique in bringing together the regulatory authorities and pharmaceutical industry to discuss...
good
GCC countries, Drug registration regulations of Saudi Arabia, Medicinal Product Registration proces...
In this slides contain a ICH guidelines process and information about the organization. https://www....
ICH GUIDELINES, ICH, INTERNATIONAL CONFERENCE ON HARMONIZATION, B PHARMA 6TH SEM, PHARMACEUTICAL QUA...
It involves origin, evolution, objectives,
ICH Guidelines
REGULATORY AFFAIRS
