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. Fulfills GWAR requirement

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.

Class Schedule | Syllabus Information | University Bookstore