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Instruction in Monitoring, Procedures Documentation and (IMPACT) Workshop: Session 1 • Monitoring for Clinical Trials

  • BSRB Seminar Rooms A, B and C (map)

Have you completed basic instruction in clinical research but are looking for more? The Instruction in Monitoring, Procedures Documentation and (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. Maximum benefit will be gained by attending all three sessions, but it is not required. All sessions are held at BSRB Seminar Rooms A, B and C.

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

Session 1: Monitoring for Clinical Trials
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.

Other topics include: 

  • Session 2: Procedures Documentation for Clinical Trials (May 17)
  • Session 3: and It's Interaction with Protocols, Documents and Study Management (May 31)

Registration is required - register here.