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 LibrarySpeakers: 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.Click here to purchase contact hour.
With more than 20,000 members, the Association of Clinical Research Professionals (ACRP) is the only non-profit solely dedicated to representing, supporting, and advocating for clinical research professionals. ACRP supports individuals and life science organizations globally by providing community, education, and credentialing programs. Founded in 1976, ACRP is a registered 501(c)(3) charitable organization whose mission is to promote excellence in clinical research and whose vision is that clinical research is performed ethically, responsibly, and professionally everywhere in the world.
CONTACT US > FAQs > JOIN OUR MAILING LIST >
JOIN THE CONVERSATION
When you become an ACRP member, you’re joining a network with a global reach—and so much more. EXPLORE THE BENEFITS OF MEMBERSHIP