This session will introduce participants to best practices in preparing for and participating in clinical trial monitoring visits. Topics will include understanding the purpose of monitoring and how it differs from an audit, what to expect from different types of monitoring visits, and tips on responding to follow-up letters and reports.

The primary audience for this session is 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.

When: Thursday, May 13
Time:10 a.m.-noon
Where: This session will be held online, and the organizers will be in touch with more information after you register.

Register here for this workshop.

***Our aim is to provide an outstanding experience for all attendees. If you require reasonable accommodations to attend this workshop, please contact the organizer at least 2 weeks in advance of the event.