Required Courses (16 q.h.)

RGA 6220	Global Biotechnology Product Registration: EU, U.S., and Japan	4 q.h.
RGA 6221	European Union Compliance Process and Regulatory Affairs	4 q.h.

Choose two of the following courses:

RGA 6228	Managing International Clinical Trials	4 q.h.
RGA 6222	Global Awareness: European Medical Device Regulations	4 q.h.
RGA 6223	Global Awareness: Canada, Asian, and Latin American Regulatory Affairs	4 q.h.
RGA 6225	Japanese Medical Device Regulations and Registrations	4 q.h.
RGA 6226	Canadian and Australian Medical Device Regulation	4 q.h.
RGA 6227	Global Awareness: Emerging Medical Device Markets	4 q.h.
RGA 6210	Strategic Planning and Project Management for Regulatory Affairs Professionals in Domestic and International Markets	4 q.h.
RGA 6212	Safety Sciences 1: Introduction to Safety and Surveillance for Drugs, Biologics, and Medical Devices in the U.S. and Abroad	4 q.h.

 

Total Quarter Hours: 16