SMPD 281A - Clinical Development Seminar I

3 units
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.

Satisfies GWAR: Graduation Writing Assessment Requirement.

Prerequisite(s): Admission to MPDM program or certificate.
Grading: Graded

Note(s): This course satisfies graduate-level GWAR in this master’s program.

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