Clinical Development Seminar II
Current practices for medical product development and the clinical and regulatory pathways required for approval in the USA; including non-clinical study design and GMP process. Emphasis on oral and written communication. Presentations from experts in the field. Prerequisite: Admission to the Medical Product Development Management program and completion of SMPD 281A. Misc/Lab: Lecture 2 hour/Activity 4 hours. Note: This course satisfies graduate-level GWAR in this master's program.
Normal Grade Rules