The lack of appropriate representation in subject populations is a long-standing challenge for clinical research. The IRB plays a central role in considering and promoting diversity and inclusion in human subjects research. This webinar reviews the rationale for improving diversity and inclusion in clinical studies and discusses how the IRB can promote diversity during routine reviews of clinical research protocols. Case examples and practical resources are presented.

 

Agenda

This webinar discusses the following topics:

  • The Belmont principle of justice and the scientific merits of inclusion.
  • Practical actions IRBs can take to promote diversity in subject populations.

 

Audience

This webinar applies to anyone involved in the design, review, or execution of clinical research protocols. IRB professionals, IRB members, researchers, and study staff will benefit from understanding the importance of diversity and inclusion in research as well as learning about tools to achieve a diverse subject population.

Seminar Information
Seminar Date:
November 10, 2020
Seminar Objectives
  • Understand the importance of diversity in clinical research and identify the scientific merits of inclusion.
  • Describe the Belmont principle of justice as the basis for the inclusion of a diverse study population.
  • Implement specific actions IRBs can take when requesting, reviewing, and responding to clinical study information that promotes the inclusion of a diverse study population.
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