A DNA double helix against a colorful background with music scales.
薬事規制関連支援サービス Sponsored Webcast

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

In this RAPS-hosted webinar, Citeline explores the case for a global, holistic framework that captures overlapping and interdependent obligations through a coordinated strategy.

Learn why managing trial disclosure by country creates gaps, duplication, and missed obligations and why a global "fishing net" strategy captures overlapping requirements more effectively than a single line.

About the event

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.

Consider this: if a regulator questioned one of your trials tomorrow, could any single person in your organization account for every disclosure obligation it carries worldwide? As disclosure requirements continue to evolve, with authorities demanding greater transparency across diverse registries, timelines, and enforcement frameworks, this siloed model is no longer sustainable.

This webinar will make the case for a "fishing net" approach: a global, holistic framework that captures overlapping and interdependent obligations through a coordinated strategy. Rather than asking "What does Country X require?" in isolation, sponsors will learn to consider how a single disclosure activity can support obligations across multiple jurisdictions, where WHO primary registry status and ICMJE recognition deliver cross-border value, and where specific local requirements still demand targeted, non-substitutable action. Drawing on the latest disclosure developments and emerging trends, we will explore how an integrated strategy reduces duplication, strengthens compliance, and keeps trial information accurate and consistently available across global platforms. By shifting from a reactive, jurisdiction-by-jurisdiction model to a strategic global approach, sponsors can cast a single "catch all" net that captures the widest possible reach.


Our session

SEP 29, 2026
11am EDT

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

This webinar will make the case for a global, holistic framework that captures overlapping and interdependent obligations through a coordinated strategy.

Learn why managing trial disclosure by country creates gaps, duplication, and missed obligations and why a global "fishing net" strategy captures overlapping requirements more effectively than a single line.

SPEAKERS
  • Headshot of Thomas Wicks.
    Thomas Wicks Head of Transparency Operations, Citeline
  • Headshot image of Ben Evans
    Ben Evans Director, Regulatory Intelligence, Citeline

Featured speakers

Headshot of Thomas Wicks.

Thomas Wicks

Head of Transparency Operations, Citeline

ライフサイエンス分野で20年以上の経験を持つ戦略リーダーであり、現在はCitelineの透明性業務責任者を務めています。業界をリードするTrialScopeの情報開示ソリューションの戦略を指揮し、透明性に関する深い知識と実績を持っています。

トーマスは、情報開示要件や透明性のトレンドについてのオピニオンリーダーとしても高く評価されており、これまでに60以上のカンファレンスで講演し、40以上の出版物を執筆しています。また、裁判の透明性を尊重するソリューションを加速させることを使命とし、チームに力を与えることに情熱を注いでいます。

Headshot image of Ben Evans

Ben Evans

Director, Regulatory Intelligence, Citeline

Ben Evans leads the development and evolution of TrialScope Intelligence, a global clinical trial regulatory intelligence platform that delivers high-quality, actionable content to help clients navigate complex disclosure regulations. His role combines research, strategy, and cross-functional collaboration, working closely with regulatory experts, product, tech, and commercial teams to ensure alignment with client needs and company goals.