This webinar invited you to pause and reflect on the ethical foundations that safeguard human participants in research. We explored the historical milestones that shaped today’s protections, examining how past research abuses led to the creation of oversight structures like the Belmont Report and Institutional Review Boards (IRBs).
David Burrow, PharmD, JD, explored foundational principles of Quality by Design (QbD), including Critical to Quality (CTQ) factors and Risk-Based Quality Management Systems (RBQM). Participants gained strategic insights into how to enhance trial quality while reducing regulatory uncertainty through forward-thinking approaches and practical tools.
This webinar provides a comprehensive guide to developing, implementing, and maintaining effective SOPs tailored to the unique needs of research sites. Attendees learned practical strategies to streamline processes, enhance regulatory compliance, and foster team collaboration.
This package is a replay of 74 on-demand session recordings and presentation slides from the ACRP 2025 Conference, April 24 – 27, New Orleans, Louisiana. It includes content from the six educational tracks, the Signature Series sessions, and techXpo sessions, presented by a variety of clinical research service providers.
A replay of 28 on-demand session recordings and presentation slides from the Study & Site Management Journey at the ACRP 2025 Conference, April 24 – 27, New Orleans, Louisiana. Learn practical, proven ways to maximize study and site performance.