
In today’s ACT Brief, we examine why the future of AI in trials is a trusted orchestration system rather than a single model, how coordinators rate eSource-enabled workflows, and what a bipartisan bill proposes for reusable trial networks.
With recent FDA Guidance on Clinical Trials COVID-19 suggesting, “If planned on-site monitoring visits are no longer possible, sponsors should consider optimizing the use of central and remote monitoring programs to maintain oversight of clinical sites," Risk-Based Quality Management (RBQM) solutions provider Cyntegrity is offering its special






