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Best Practices for Safety Reporting in Clinical Trials for Drugs, Biologics and Medical Devices

June 14 @ 9:00 am - June 15 @ 6:00 pm

This seminar begins with outlining the structural role of the FDA and a brief introduction to the Food, Drug and Cosmetic Act (the ACT) and how the FDA uses it to enforce the regulatory requirements during the drug, biologics and medical device approval process. Additionally, this seminar will highlight safety, which is in the FDA’s mission statement and by guiding participants on how to develop a data safety monitoring plan.

Details

Start:
June 14 @ 9:00 am
End:
June 15 @ 6:00 pm
Website:
http://bit.ly/Clinical-Trial-Practice-for-Drugs-and-Biologics

Organizer

Event Coordinator
Phone:
+1-800-447-9407

Venue

Four Points By Sheraton
1617 1st Avenue
San Diego, CA 92101 United States
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