Key Documents and Software in Clinical Research
Get familiar with the key documents that must be completed during a clinical trial. Working knowledge of these important components is crucial to mastering future role in research.
In clinical trials, Essential Documents refer to regulatory documents that serve to demonstrate the compliance of the Investigator, Sponsor, and Monitor with the standards of Good Clinical Practice (GCP) and with all applicable regulatory requirements.
About 45 Minutes
Self-Paced
$49
Introduction to Clinical Research Part 5
Key Documents and Software in Clinical Research
Essential Documents in a Clinical Trial: Video
Essential Documents: 10-page pdf document
Software Systems in Clinical Research: 7-page pdf document