If you work in clinical trial disclosure, it’s imperative that you understand the growing global landscape of regulatory requirements.
This three-part webinar series, Global Clinical Trial Transparency — from Compliance to Emerging Requirements, takes you from disclosure fundamentals to the trial registry ecosystem to plain language summaries.
Together, the sessions build a comprehensive foundation for insight into global clinical trial disclosure compliance.
Learn from regulatory expert Ben Evans, Citeline Disclosure Regulations Research Manager, who will share his expertise on global disclosure regulations — and how to maintain compliance.
Webinar Series
Wed Aug. 20 10AM EST | 3PM BST
Global Clinical Trial Disclosure Fundamentals – Requirements, Timing, and Enforcement Consequences
Catch up on core disclosure requirements: what must be disclosed, when, and how. Learn about enforcement mechanisms and why maintaining compliance is crucial.
Key Learnings:
- Understand core disclosure requirements and timelines across global jurisdictions
- Identify potential penalties for noncompliance
Wed Aug. 27 10AM EST | 3PM BST
Navigating the Clinical Trial Registry Ecosystem — Regional and Global Registry Selection
This webinar is your GPS for the complex landscape of clinical trial registries, including registry-specific requirements. Your journey will include harmonization initiatives aimed at improving transparency and data consistency across registries.
Key Learnings:
- Differentiate between global, regional, and national registry requirements
- Determine key factors in selecting appropriate registries for multi-jurisdictional studies
Wed Sept. 3 10AM EST | 3PM BST
Beyond Clinical Trial Registration — Plain Language Summaries
Discover the growing importance of plain language summaries (PLS) as a requirement in global transparency. Focusing on both protocol and results summaries, this session will also cover evolving regulatory expectations and best practices for global PLS implementation.
Key Learnings:
- Gain an overview of regulatory PLS requirements across regions
- Garner insights into varying expectations for protocol and results summaries
- Learn how PLS fit within global clinical trial disclosure frameworks