Changes in ICH GCP with the Upcoming Revision 3
18:18
Risk-based Monitoring - Risk-optimized approaches to clinical trials - Introduction - Part 1 of 3
16:44
What’s NEW in ICH GCP E6 R(3) Guideline? Key Changes & Implications for Clinical Researchers #gcp
2:13
¿Vale la pena hacer Erasmus?
8:53
The Basics of Essential Documents in the Trial Master File – Part 1 - Before the Clinical Phase
23:41
Clinical Research Associate (CRA) Job Responsibilities
15:42
Principles of Clinical Trial Management
58:13
Good Clinical Practices -General Tips by Jacquelyn Legere, HRPP Director
42:31