Coronavirus (COVID-19) Update
All ongoing and spring classes have been moved to a remote format. Please check our coronavirus update page for our latest announcements.
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:
|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|
Ask us any questions you may have about this course.