Intermediate CRA Training - Houston

This two-day seminar, worth 12 contact hours, is recommended for clinical research associates (CRAs) or others who are interested in monitoring clinical trials. It is designed for the professional who has more than a basic knowledge in the area of clinical trial management. Course topics include regulatory compliance, principles of case report form development and advanced clinical monitoring. Enrollment is limited to 55 participants.

Get more information about this course, including course objectives, an agenda and staff.