Patient-Oriented Research Certification Program

Dawn Ziegmann
To complete certification, you must review each module and complete the quiz at the end of each module with a score of 85% or better. You will be provided with a link to the quiz upon completion of the module materials. It is recommended that you complete the modules in order.
Adobe PDF of Lesson Materials View Resources
ER = Required for Expedited Review Certification
FR = Required for Full Review Certification
ER FR Module Anticipated Time Module Status Quiz Status
Historical Perspectives on Human Subject Protection 45 min Completed Content, Pending Quiz
(Revisit Module) 		(Take Quiz Now)
IRB and Federal Regulations Overview 45 min Not Started
(Begin Module) 		 
Conflict of Interest 20 min Not Started
(Begin Module) 		 
  Introduction to Good Clinical Practices 30 min Not Started
(Begin Module) 		 
  FDA Regulations for Clinical Research (IND/IDE) 20 min Not Started
(Begin Module) 		 
  Informed Consent 20 min Not Started
(Begin Module) 		 
  Adverse Events 20 min Not Started
(Begin Module) 		 
  Data and Safety Monitoring 20 min Not Started
(Begin Module) 		 
  FDA Audits 20 min Not Started
(Begin Module) 		 
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