Global Clinical Trial Disclosure: Are You Casting a Line or a Net?

Clinical trial disclosure is typically managed at the jurisdiction level, with teams treating each country’s registration and results-posting obligations as separate, isolated tasks. The “fishing line” approach, managing each requirement individually, may appear efficient on the surface, but can introduce significant risks:

• Duplicated effort, as teams repeat work that could satisfy multiple jurisdictions at once
• Inconsistent records across registries and public platforms
• Missed obligations, when no single team holds a comprehensive view of global requirements.