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2020 MBA - Pharmaceutical Management Syllabus Description Overview: The 2020 MBA in Pharmaceutical M...
Basics of USDMF, Types, Modules, contents, Review and Approval
It gives information about CTD and eCTD. Also, please learn about their similarities and differences...
Designing and Implementing a Regulatory Programme for Medical Devices
Tender application in the ROW market
Good clinical practice ICH GCP E6
Mechanisms of drug release from microspheres and microcapsules
Consultores en Asuntos Regulatorios
MICROSPHERES AND THEIR PHARMACEUTICAL APPLICATION
- Whilst the realization of the CTD took many years, there is now a common format for the submission...
NON CLINICAL DRUG DEVELOPMENT
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This presentation, “Phase 0 Trials by Dr. Surya K,” is designed to offer a clear, structured, an...
Medical Affairs Functions in Pharmaceutical Companies: Mission, Activities, Processes, and Challenge...
FDA
This presentation explains in brief the process, types, requirements, and conditions where PAS is ne...
Project work ppt
Medical device regulation is complex, in part because of the wide variety of items that are categori...
Different organization of US FDA and its responsibility.
QRM in Pharmaceutical Industry, ICH Guideline - Q9
A Presentation about D&C Act 1940 - Schedule Y, Amendment 2005 by Akshay Anand, covering aspects...
Pharmaceutical regulatory affair is the interface between pharmaceutical industry and the regulatory...
East African Community (EAC Committee Organization)
