MRA 610A Regulatory Affairs Capstone
Lead Faculty: Mr. Irvin Kluth
A two month course that meets on a once a week basis, this course is designed to have the student develop and implement a research document that integrates all facets of a clinical trial including regulations, documentation, clinical evidence, data management, statistical analysis of the data and other principles taught throughout the entire program. Grading is by S or U only. Course is eligible for an "IP" grade.