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SMPD 281A

Clinical Development Seminar I

Description
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.

Grading
Normal Grade Rules

Units
3