The Basics of Essential Documents in the Trial Master File – Part 1 - Before the Clinical Phase
5:55
The Basics of Essential Documents in the Trial Master File – Part 2 - During the Clinical Conduct
13:41
Investigator Site File: A Comprehensive Guide to Clinical Research Documentation
7:31
CRA Basics: What is Risk-Based Monitoring in Clinical Research?
6:59
QA, QC and Audits in Clinical Trials: What is the Difference?
5:18
The Basics of Essential Documents in the Trial Master File – Part 3 - After the Clinical Phase
6:59
Understanding Clinical Trials
10:59
Changes in ICH GCP with the Upcoming Revision 3
15:42