05.13.26 -- STREAM Edition: Watch Presentations The Help You Grow And Improve Clinical Trials

Scale logistical support to eliminate site burdens and participant friction. Whether managing global travel or routine reimbursements, seamless coordination keeps your study moving forward.

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.

Leveraging primary care for chronic disease studies can accelerate patient identification, access to underrepresented populations, and improve retention rates.

This clip explores how rigid RTSM systems push teams into risky manual workarounds and highlights why flexible, adaptable technology is essential when studies evolve and operational demands shift.

Gain an auditor’s insight into common compliance gaps and learn practical ways to strengthen audit readiness in sIRB studies. 

The data that you use to train AI models has to be “fit for use” according to the FDA. Tala Fakhouri explains what metrics the FDA uses to make this determination.

Central eSource transforms the conduct of clinical trials by replacing disparate, site-specific source templates with a unified, sponsor-designed framework.

Explore how natural language queries enable instant clinical listings while maintaining oversight, as well as what becomes possible when teams reduce manual effort without sacrificing control.

Practical examples of RWE, according to Kathleen Mandziuk, include improving trial design, by refining I/E criteria, reducing patient burden, and using real-world behavior data. She highlights how mismatches between protocol demands and real patient lives can hurt recruitment and retention.