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Webinar | Research Misconduct in Clinical Trials/OIG/OCR

Description

Essential Components of a Clinical Trial Agreement | Webinar Series

Research misconduct is the bane of the research community. It destroys trust in science and the promise of science which should be the search for truth. This betrayal is most keenly and immediately felt when researchers conducting a clinical trial do not have integrity. The fallout for an institution when research misconduct is found during a clinical trial is significant. This webinar will explore which of those ethical breaches in the context of a clinical trial rise to the level of research misconduct and which do not (at least in the United States). We will explore these concepts through a review of illustrative cases finding research misconduct.

Learning Objectives:

  1. Identify which problems in clinical trials rise to the level of research misconduct and the follow therefrom.
  2. Understand the civil and criminal causes of action against lower level researchers and principal investigators who commit research misconduct in a clinical trial.
Knowledge Level: All Levels

Registration
(Deadline May 22)
Late Registration***
(After May 22)

Individual Registration
Member Rate* $99 $114
Non-Member Rate $165 $180
Group Registration**
Member/Non-Member Rate $350 $365

Register for the entire Webinar Series for one low rate!

Registration includes access to the live event, PowerPoint slides, and complimentary access to the On-Demand version for 30-days.
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**All Group Attendees must be added when registering. Up to 12 attendees per group.
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Contributors

  • Debra Parrish, Partner, Parrish Law Offices, LLC

    Ms. Parrish is an attorney who works with academic medical centers, research institutions and companies, particularly those in the life sciences area in the United States. Her areas of legal concentration are science law (including research misconduct, regulations, compliance and investigations), health care law, and intellectual property. Ms. Parrish previously worked at the Office of Research Integrity as an attorney and now counsels journals, institutions and scientists on matters of research integrity. She is a frequent speaker and author on research integrity issues and has worked on some of the most high profile and complex cases over the past 25 years. In March 2016 she served as an invited panel member on research integrity issues at the National Academy of Sciences. She received her law degree and bachelor of science in biomedical engineering from Duke University and is a member of the patent bar.

May 23, 2024
Thu 2:00 PM EDT

Duration 1H 0M

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