The Association of Clinical Research Professionals

Diverse Women in Clinical Trials Webinar Series

In conjunction with the U.S. Food and Drug Administration, ACRP presents a webinar series addressing strategies for increasing recruitment and retention of diverse populations of women in clinical trials.

 

Join FDA Commissioner Robert M. Califf, MD, for an overview of FDA’s initiatives to increase clinical trial participation among diverse populations. FDA officials and experts in the field will then provide guidance on diversity planning, recruitment, and retention, with specific focus on diverse women.

In a third webinar, FDA officials will reveal best practices for preparing for FDA inspections and key strategies for responding to Form FDA 483s.

Planning for Diversity | November 1

12:00 – 1:00pm EDT

Attendees will learn new approaches to boost recruitment and retention by creating research environments that foster effective communication and outreach to diverse populations of women.

Speakers include Marjorie Jenkins, MD, MEd, FACP, Director of Medical Initiatives and Scientific Engagement, Office of Women’s Health, FDA, and Aisha Langford, PhD, MPH, Assistant Professor of Population Health, New York University School of Medicine.

Details & Registration

Recruitment and Retention | November 9

12:00 – 1:00pm EDT

Attendees will learn practical strategies for overcoming the barriers that can derail recruitment and retention of diverse populations of women.

Speakers include Marjorie Jenkins, MD, MEHP, FACP, Director, Medical Initiatives and Scientific Engagement, FDA’s Office of Women’s Health.

Details & Registration

FDA BIMO Compliance and Enforcement of Drugs and Devices | November 16

12:00 – 1:00pm EDT

Attendees will learn best practices for preparing for FDA inspections and key strategies for responding to Form FDA 483s.

Speakers include David Burrow, PharmD, JD, Acting Director of the Office of Scientific Investigations, Center for Drug Evaluation and Research Office of Compliance, FDA, and CDR Tamika Allen, MS, RN, Senior Regulatory Operations Officer and Premarket Team Lead, Center for Devices and Radiological Health Division of Bioresearch Monitoring, FDA

Details & Registration