Global Clinical Trial Disclosure: Are You Casting A Line Or A Net?

Teams typically manage clinical trial disclosure at the jurisdiction level, treating each country's registration and results-posting obligations as separate, isolated tasks. This “fishing line” approach of managing each requirement individually may appear efficient on the surface, but it can introduce significant compliance risks, including duplicated effort, inconsistent records across registries and public platforms, and missed obligations.

Disclosure requirements continue to evolve, and authorities demand greater transparency across diverse registries, timelines, and enforcement frameworks, making the siloed model no longer sustainable. This on-demand webinar makes the case for a “fishing net” approach: a global, holistic framework that captures overlapping and interdependent obligations through a coordinated strategy. Sponsors will learn to consider how a single disclosure activity can support obligations across multiple jurisdictions, where World Health Organization (WHO) primary registry status and International Committee of Medical Journal Editors (ICMJE) recognition deliver cross-border value, and where specific local requirements still demand targeted, non-substitutable action.