MCR 7460
Regulatory Strategy and Clinical Trial Reporting
Explores regulatory strategy in new medical product development and the roles of regulatory professionals. Scholarly and technical writing skills for regulatory professionals for new product submissions and Food and Drug Administration (FDA) Advisory Panels. Principles of strategic planning, leadership, communication, and team building. Prereq: Enrollment in MCR program; or permission of instructor.
Sources
- Course catalogue ↗Current public catalogue; retrieved 2026-11-05