Signature Series Session
Clinical research is undergoing a dynamic transformation—propelled by breakthrough developments, evolving regulations, and fresh approaches to collaboration. In this fast-moving landscape, adaptability and strategic foresight are no longer optional—they’re essential for navigating what’s next.
David Burrow will offer strategic insights on elevating trial quality and minimizing regulatory uncertainty—sharing forward-thinking approaches and practical tools designed to help research professionals thrive in today’s complex and rapidly shifting environment.
Key topics:
Emerging trends shaping the future of clinical research
Foundational principles of Quality by Design
Leveraging the FDA’s CDER Center for Clinical Trial Innovation (C3TI)
The growing impact of artificial intelligence on trial design and execution
Actionable strategies for navigating periods of rapid change
Whether you're rethinking trial design, exploring new technologies, or seeking clarity in a changing regulatory landscape, you’ll leave this session equipped to lead with purpose and drive meaningful progress in a field that’s redefining what’s possible.
CEU: 1.00 ACRP
Speaker:
David Burrow, PharmD, JD, Director, Office of Scientific Investigations, U.S. Food and Drug Administration