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Evaluating Payment to Participate in Research: Ethical and Regulatory Issues

Evaluating Payment to Participate in Research: Ethical and Regulatory Issues

Wednesday, April 26
Presentation: 2:00-3:00pm ET
Q&A: 3:00-3:15pm ET

According to the US Office for Human Research Protections (OHRP), paying individuals to participate in research is a “common and, in general, acceptable practice.” At the same time, both the Common Rule and FDA regulations instruct researchers and IRBs to minimize the possibility of coercion and undue influence during informed consent, which has often been interpreted as placing limits on acceptable payment amounts.

In this webinar, Luke Gelinas, Petrie-Flom Center/Harvard Catalyst Fellow in Clinical Research Ethics at Harvard Law School and Schulman IRB member, proposes a practical framework for evaluating offers of payment and applies it to case studies to yield guidance on challenging ethical and regulatory issues involved in paying research subjects.

Presentation Objectives
In this free webinar, we will:

  • Analyze case studies aimed at drawing out challenging ethical and regulatory aspects of paying research subjects
  • Define the key regulatory terms of “coercion” and “undue influence” and the main risk of payment in relation to these concepts
  • Describe and apply a practical framework for evaluating payment that stresses the importance of being clear about why payment is being offered: as reimbursement, compensation, or recruitment incentive.

Who Should Attend

  • IRB members of any experience level
  • Principal Investigators and research staff
  • Site or sponsor personnel (or others) involved with proposing payment amounts or setting policy around payment

Certificates of attendance are available for this event. This presentation may qualify for continuing education credits; check with your certifying organization(s) for more information.

Space is limited–register now!

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