10.21.26 -- From Protocol Design To Site Workflows: Building Trials That Run Smarter

Master the complexities of renal and hepatic trials by leveraging site expertise and PK modeling to navigate recruitment challenges and ensure precise dosing for impaired populations.

New global research shows how sites prepare source documents, where inefficiencies occur, and why workflows differ — highlighting ways to streamline processes, cut delays, and improve data quality.

Selecting the right functional service provider (FSP) is a critical factor in advancing clinical research programs efficiently, and this reimagined FSP model prioritizes each client’s unique objectives.

Clinical study management has fundamentally changed. This video explores why the traditional top-heavy approach must give way to more efficient, adaptable products.

Learn how protocol choices like AI, adaptive designs, and decentralized methods impact IRB review, participant protections, consent, and key regulatory requirements in clinical research.

Learn how to translate ICH E6(R3) into practice with actionable strategies for proactive risk management, robust data governance, and earlier deviation detection.

Explore the platform serving as a neutral aggregator, connector, and communicator of the key systems and tasks your research site needs.

Sophia McLeod, advocacy advisor, at ACRO, explains what ACRO members are concerned about regarding the FDA staffing losses. She also talks about the effects of "policy by press release" rather than traditional notice-and-comment periods.