Clinical Trials Site Monitoring I

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.


Sections Open for Enrollment:

Open Sections and Schedule
Start / End Date Units Location Cost Instructor
04-15-2020 to 05-06-2020 2.0 ONLINE $785

Karim N Sajwani



Date: Start Time: End Time: Meeting Type: Location:
Wed, 04-15-2020 6:00 p.m. 9:00 p.m. Live-Online ONLINE
Wed, 04-22-2020 6:00 p.m. 9:00 p.m. Live-Online ONLINE
Wed, 04-29-2020 6:00 p.m. 9:00 p.m. Live-Online ONLINE
Sat, 05-02-2020 10:00 a.m. 4:00 p.m. Live-Online ONLINE
Wed, 05-06-2020 6:00 p.m. 9:00 p.m. Live-Online ONLINE

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