Clinical Trials Site Monitoring | CTDM.X404

This course presents the essential elements of monitoring a clinical trial and the interaction between a sponsor and one or more sites during a clinical investigation. The course covers expectations of the FDA, the sponsor, and the site. The process of site selection, budgeting, initiation visits, source documentation, regulatory documentation, and adverse event reporting are additional topics covered. Included in the course are the process of medical record review and maintenance, case report form completion, product accountability, and various tasks associated with different monitoring visits.

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

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This course is related to the following programs:


Sections Open for Enrollment:

Open Sections and Schedule
Start / End Date Units Meeting Type Cost Instructor
05-03-2021 to 06-07-2021 2.0 Online $660

Karim N Sajwani



Date: Start Time: End Time: Meeting Type: Location:
Mon, 05-03-2021 12:01 a.m. 11:59 p.m. Online ONLINE
Mon, 06-07-2021 12:01 a.m. 11:59 p.m. Online ONLINE