Where Policy Meets Practice in Clinical Research

Clinical research policy continues to shape how studies are designed, conducted, and managed across the research ecosystem.

This webinar explores how policy decisions and regulatory priorities influence clinical trial operations, site workflows, technology adoption, and participant access. Through a discussion of both the broader policy landscape and real-world operational impact, clinical research professionals can better understand policy shifts, anticipate downstream effects, and engage more thoughtfully in conversations that shape the future of clinical trials. Gain insight into how policy connects to everyday research practices—and why staying informed is essential to supporting compliant, efficient, and patient-centered research. 

Learning Objectives:

Upon completion of this continuing education program, participants should be able to:

1. Describe current policy, legislative, and regulatory developments influencing clinical research in the United States.
2. Explain how federal funding, workforce capacity, agency resources, and global competition affect clinical trial operations and timelines.
3. Examine how modernization initiatives involving technology, data interoperability, decentralized research, and streamlined regulatory processes may influence trial conduct.
4. Recognize how policy decisions can affect research sites, participant access, workforce sustainability, and the global competitiveness of U.S. clinical trials.
5. Identify opportunities for clinical research professionals to contribute operational insight to policy and advocacy discussions.

Speakers:

• Catherine Gregor, MBA, CCRP, CCRC, Chief Clinical Trial Officer, Florence Healthcare
• Sophia McLeod, Director, Government Relations, Association of Clinical Research Organizations (ACRO)

Approved for 1.0 ACRP Contact Hours