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IMPACT: Monitoring for Clinical Trials

  • Michigan Institute for Clinical & Health Research (MICHR) 1600 Huron Parkway, Building 400 Ann Arbor, MI 48109 (map)

Have you completed basic instruction in clinical research but are looking for more? The Instruction in Monitoring, Procedures Documentation and ClinicalTrials.gov (IMPACT) workshop series is designed for study team members who are ready for an intermediate level of training for clinical trials skills. Participants will learn critical clinical research skills through a group learning environment and hands-on skills practice.  Sessions will be virtual and information will be emailed to registrants before the event. Note all sessions will have separate registrations.

Brought to you by the Michigan Institute for Clinical & Health Research (MICHR) and the Clinical Trial Support Office (CTSO).

REGISTRATION IS REQUIRED. Please register through Eventbrite.  

Session Description:

Monitoring for Clinical Trials

October 28, 2021 - 1-3 p.m.     

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.