The Association of Clinical Research Professionals

The Changing Face of Vulnerable Subjects: Current Regulations and Guidance

Regulation states that ultimate responsibility for a clinical trial rests with the principal investigator. But what happens when a coordinator “goes rogue” and is guilty of misconduct? The speaker will explore the definition of misconduct in clinical trials and the possible consequences of intentional misconduct by a coordinator. Hear actual case studies delineating coordinator sanctions and punishments, as well as reasons for committing fraud.

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This program is a recorded session from ACRP 2018