Home / Resources / RAPS Sponsored Webcast: Global Clinical Trial Disclosure - Are you Casting a Line or a Net?
ON DEMAND WEBINAR | OCT 09, 2026

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.

This session examines the growing complexity of global clinical trial disclosure requirements and highlights practical strategies organizations can use to stay compliant while improving operational efficiency.

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5 Key Takeaways
  • Understand your global disclosure footprint
  • Look beyond regulatory requirements
  • Stay ahead of regulatory change
  • Maintain sponsor oversight
  • Build a scalable disclosure framework
Featured speakers
Headshot of Thomas Wicks.
Thomas Wicks
Head of Transparency Operations
Citeline
Headshot image of Ben Evans
Ben Evans
Disclosure Regulations Research Manager
Citeline
Thomas Wicks
Head of Transparency Operations
 Citeline
Thomas Wicks is the Head of Transparency Operations at TrialScope, a Citeline company, where he coordinates TrialScope’s operations, consults on the business strategy, and leads the disclosure advisory services. He is responsible for tracking clinical disclosure and data-sharing trends that shape the company’s clinical transparency solutions and services. Thomas has over 25 years of experience with compliance management solutions, specializing in applications for life sciences with a focus on clinical trial disclosure and transparency since 2007.
Ben Evans
Disclosure Regulations Research Manager
 Citeline
Benedict Evans is a regulatory professional with expertise in clinical trial disclosure, medical technology, and biotechnology.

As Disclosure Regulations Research Manager at Citeline, Benedict works on the content development and expansion of TrialScope Intelligence, ensuring that sponsors have access to reliable, up-to-date regulatory insights to inform actionable regulatory intelligence. With a strong foundation in science, regulation, and project management, Benedict has worked across the biotech, life sciences, and medical technology sectors, helping organizations navigate regulatory requirements.