Found 202 presentations matching your search
Unit 2 Regulatory Approval Process Approval processes and timelines involved in Investigational New...
Regulatory authority of japan
It gives information about CTD and eCTD. Also, please learn about their similarities and differences...
Regulatory affairs, introduction, History, DRA
*RA or government affairs, is a profession involved in monitoring and regulating the development, m...
ICH GCP guidelines for mpharmacy 2nd sem 204T subject. topic include the brief description regarding...
It is unique in bringing together the regulatory authorities and pharmaceutical industry to discuss...
Turacoz Skill Development Program provides medical writing training on various types of regulatory d...
This presentation gives knowledge on ICH and its History, Mission, and overview of ICH Quality, Safe...
REGULATORY AFFAIRS
The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human ...
COMMON TECHNICAL DOCUMENT
The ppt gives a basic information about ICH-GCP, how it originated , what led to the formation of IC...
A brief introduction to Drug Regulatory Affairs and Its Regulatory Authority.
- Whilst the realization of the CTD took many years, there is now a common format for the submission...
good
Nicely described regarding about the overview of ICH guidelines as per PCI syllabus specially for Ph...
In Japan, the pharmaceutical industry operates under strict regulatory oversight by the Pharmaceutic...
It includes information about regulatory bodies, role of drug Regulatory professional, countries wit...
This SlideShare presentation provides a comprehensive exploration of Good Clinical Practice (GCP) as...
A dossier refers to a comprehensive collection of documents submitted to a regulatory authority to d...
CTD eCTD organization of CTD & eCTD CTD triangle Module 1 to 5
COMMON TECHNICAL DOCUMENT , its granularities, benefits, advantages, shortcomings.
