CRA Basics: What is Risk-Based Monitoring in Clinical Research?
5:25
Understanding the Basics: Data Management in Clinical Research
5:34
CRA Basics: The Purposes of Clinical Trial Monitoring
10:59
Changes in ICH GCP with the Upcoming Revision 3
8:53
The Basics of Essential Documents in the Trial Master File – Part 1 - Before the Clinical Phase
6:06
What is Centralized Statistical Monitoring in Clinical Research?
9:28
Preparing for Regulatory Authority Inspections in Clinical Trials
6:37
The Role of a Clinical Project Manager in Clinical Trials final
18:18