Clinical Trials Site Monitoring II

This course explores a range of approaches to monitoring clinical sites, the development of monitoring plans, and some of the more challenging aspects of monitoring clinical trials. Remote data entry, compliance audits, regulatory issues that arise in compliance audits, fraud and misconduct are also addressed. This course is designed for clinical research associates (CRAs) or those planning to become a CRA, clinical trial managers and clinical operations managers.

Professional Credit: CA BRN/LVN Credit--Provider #CEP13114.


Prerequisites :

Offering code Offering title
CTDM.X404 Clinical Trials Site Monitoring I