Applying the FDA Framework in Conducting IRB Review

Virtual presentation co-presented by the UK Office of Research Integrity (ORI) and the UK Center for Clinical and Translational Science (CCTS)
   
Objectives:

Examine when an activity falls under FDA regulations.
Outline a step-by-step framework for applying FDA regulations in clinical investigations.
 

Suggested audience:
IRB members, IRB staff. Clinical Research Investigators, Research Coordinators, Research Regulatory Personnel
   
No registration required. Does not qualify for continuing education credit.