RGAF 6250 - Regulatory Clinical Evidence

Credits: (2)
Typically Taught Spring Semester: 2nd Block Online
Description: The evaluation and assessment of regulatory strategies that include protocol development, study design, post-marketing surveillance, evaluation and, assessment of regulatory submissions. Utilizing clinical trial design, participants will evaluate and assess strategies for achieving regulatory goals. Students are introduced to requirements of planning and conducting clinical trials. Clinical trial terminology and design are discussed including planning and carrying out a study.
Pre-requisite(s): RGAF 6000