Trial Misconduct: Examples and Implication for Your Clinical Staff

When:  Jun 6, 2022 from 05:15 PM to 07:00 PM (MT)
Associated with  ACRP Front Range Chapter

The Buck Stops with the PI... or Does It? Regulation states that ultimate responsibility for a clinical trial rests with the principal investigator. This session will provide information on the implications and consequences of investigator and staff misconduct in clinical research. Using case studies and actual findings, participants will learn about clinical trials compliance, what kinds of misconduct have occurred in the past and the consequences of a finding of misconduct. Reasons for committing fraud will be explored.

This presentation is a webinar replay from the ACRP Online Conference Library

Speakers: Michael Hamrell, RAC, CCRA, RQAP-GCP, PhD, President, Moriah                              Consultants
                 
Janet Holwell, CCRC, CCRA, TIACR, FACRP, Independent Consultant

**Please email the contact person listed on this page to register for this event.

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Contact

Laurie Burnside
(303)722-1414
Laurie.burnside@outlook.com