On-demand Webinar

Designing representative clinical trials: Best practices and strategies for inclusion

Mike Ward
Global Head of Life Science & Healthcare Thought Leadership
Ellen Coleman, MPH, MSSA
Senior Advisor, President Emeritus
VOZ Advisors
Karlin Schroeder
Associate Vice President, Community Engagement
Parkinson's Foundation
Sara Bristol Calvert
Director of Projects
Clinical Trials Transformation Initiative (CTTI)
Lindsay Cobbs
US Policy Head
Lashell Robinson
Director of Diversity & Inclusion in Clinical Trials

In April 2022, the FDA released Draft Guidance entitled ‘Diversity Plans to Improve Enrollment of Participants from Underrepresented Racial and Ethnic Populations in Clinical Trials’.

It recommends developing and submitting a Race and Ethnicity Diversity Plan to increase participation in clinical trials by populations currently underrepresented in such studies.

Clarivate and VOZ Advisors invite you to join industry executives, patient advocates, academic center representatives, and regulatory experts in a discussion about the implications of the Draft Guidance, emerging best practices in supporting diversity in clinical trials, and developing opportunities for establishing sustainable relationships with underrepresented communities.

What will be covered in this Webinar:

  • Understand the content of the Draft Guidance, the potential impact and implications for industry and impacted communities.
  • Learn about successful efforts in improving diversity in clinical trials
  • Consider strategies for developing long lasting, mutually beneficial relationships with underserved communities.