IMPACT: Monitoring for Clinical Trials

November 13, 2018 2:00 PM to 4:00 PM
University Hospital 2nd Floor - UH Room 2C108
1500 E. Medical Center Drive
Ann Arbor, MI 48109

Instruction in Monitoring, Procedures Documentation and ClinicalTrials.gov (IMPACT) 
Have you completed basic instruction in clinical research but are looking for more? The Instruction in Monitoring, Protocols, and Advanced documentation in Clinical Trials (IMPACT) workshop series is designed 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.      

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 Sessions:
Procedures Documentation for Clinical Trials (November 7)
ClinicalTrials.gov and Its Interaction with Protocols, Documents and Study Management (November 28)

Our aim is to provide an outstanding experience for all attendees. If you require reasonable accommodations in order to attend, please find additional information on the registration page about how to request these.