Clinical Development Seminar I
Provides a comprehensive overview of the regulated medical product development process. Topics include initial drug development/device invention to drug/device approval and post-market surveillance. Discussions include non-clinical and clinical studies, regulations, clinical indication determination, research methodology and ethical conduct. Fulfills GWAR requirement Prerequisite: Admission to MPDM program or certificate Note: This course satisfies graduate-level GWAR in this master's program.
Normal Grade Rules