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Webinar: (2019-04) IRBs and Research Ethics Consultation Services: An Emerging Resource and Opportunity for Collaboration


The principal source of ethical review for human subjects research has traditionally been the IRB. For a variety of reasons, increasing numbers of institutions are developing research ethics consultation services to provide guidance to investigators, study teams, research subjects, and IRBs about ethical issues arising in particular research studies. The presence of an additional source of ethics input and guidance raises important questions about the relationships between these ethics consultation services and IRBs. During this webinar, speakers will address such questions and more. (Presented on April 23, 2019)

Agenda

  • Definition of research ethics consultation and research ethics consultation services
  • Framework for reviewing research from an ethical standpoint and how it applies to research ethics consultation services
  • Examples of consult questions that illustrate four contexts where clinical research ethics consultation may be useful:
    • Before and after regulatory review
    • Challenging and novel ethical issues
    • Increasing challenges of informed consent and risk/benefit analysis
    • Collaborative assistance
  • Anticipated challenges and opportunities for research ethics consultation services
  • Opportunities for IRBs and consultation services to complement and mutually support one another

What will I learn?

After attending this webinar, you will be able to:
  • Define the function and purpose of research ethics consultation services
  • Recognize the ways in which research ethics consultation services differ from the IRB
  • Identify opportunities for IRBs and research ethics consultation services to collaborate and support one another

Who should attend?

This webinar will benefit IRB professionals and members.

Continuing Education

Webinar participants holding the Certified IRB Professional (CIP®) credential may apply 1.25 continuing education credits towards CIP recertification. Learn More »

Thank You to our Webinar Supporter!

HRP Consulting Group
HRP Consulting Group
HRP Consulting Group provides expert advice to institutions seeking to develop or improve all aspects of their human research protection program. For more information, please visit www.thehrpconsultinggroup.com.

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Access Interval
Access to purchased content will be available for 90 days after the date of purchase. After 90 days, access to the content will be removed, but users will retain access to any certificates of attendance earned. Content purchased prior to January 1, 2021 will remain available indefinitely. After access has expired, users can purchase an additional 90 days of access.

If you'd prefer a paper form, please click here. Please send the completed form to registration@primr.org.