Join us for an interactive introduction to best practices in preparing for and participating in clinical trial monitoring visits. During this virtual program you will learn about the purpose of monitoring and how it differs from an audit, what to expect from different types of monitoring visits, preparing for an interim visit, and tips on responding to follow-up letters and reports. Participants will engage in activities in both large and small groups.
This session does not teach how to become a monitor.
Primary audience: Study team members who are involved with required monitoring visits for drug, device, or biologic clinical trials, but anyone interested in learning more about monitoring for clinical trials is welcome. This is intermediate-level training, so participants are expected to understand basic clinical trials procedures and terminology through experience or prior training.
Due to confidentiality and U-M-specific policies and procedures, this session is open to U-M employees, affiliated health systems, or those working on a clinical trial with a U-M principal investigator.
REGISTRATION IS REQUIRED [add registration link]
*If you are interested in the training and cannot attend the June 6 workshop, please sign up to be notified about future workshops at the registration link.
**We aim to provide an outstanding experience for all attendees. If you require reasonable accommodations to attend, please get in touch with the organizers two weeks before the event at [email protected].