Found 113 presentations matching your search
this ppt talks about glp principles overview, the way it is implemented in various countries, and a ...
Lets, just get to know more about safety reporting in clinical trails with some terminologies, repor...
Essential documents for conduct a clinical trials
GCP is a set of guidelines for how clinical trials should be carried out. It ensures that the data...
CT
Clinical Research and Pharmacovigilance
Supplier Training - Procurement Policy & Protocol covering topics like SRM, Procurement Policy, ...
Amendments in Schedule Y in 2013,2014 inserted three new rules, new appendix XII: compensation in c...
This presentation is a brief overview of ICH-GCP guidelines. Although ICH-GCP is a very vast topic, ...
this ppt contains about 21 CFR part 312
In any work or process documents that are needed before initiation, Between or generally the end of ...
Investigational new drug application approval process and IND detailed information//INDA//
Good clinical practice ICH GCP E6
21 CFR 312 and 314 are two separate, but related, US Food and Drug Administration (FDA) regulations ...
Crp
Dr. Merrin Joseph,Department of pharmacy practice,Institutional Review board /Research and ethical c...
This PPT give information about Institutional Human Ethics Committee
GCP course material
Drug safety reporting has a vital role in the pre-approval and post-approval phases. It is essentia...
Slides prepared for IIUM GCP Workshop
Climate change is a major issue in global politics
DEVELOPING CLINICAL TRIAL PROTOCOL
Presentation on ICH-GCP guideline.
