Ask the Expert: Protocols, clinicaltrials.gov, and Office of Research Compliance & Review

October 25, 2022 - 12:00 PM to 1:00 PM

Meet with experts from the MICHR clinicaltrials.gov team and the Office of Research Compliance & Review for advice on drafting robust protocol documents, complying with research regulations, and implementing your project at U-M.

Experts for this session include:

  • Katy Hunsche, Research Compliance Associate, Office of Research Compliance Review
  • Kate Sasamoto, Director, Office of Research Compliance Review
  • Monika Blue-Benedict, BS, CCRP, Project Manager, MICHR
  • Amy Skyles, PharmD, Assistant Director, IRBMED

The Clinical Trials Support Office's "Ask the Expert" sessions allow faculty, study teams, and staff to drop in during the hour to ask questions about their individual study or workflow needs.