The completion of a clinical document marks not the end, but the beginning, of its lifecycle. From clinical trial registries and marketing authorization submissions to post-marketing disclosure mandates (such as EMA Policy 0070 and Health Canada PRCI), your documents must be shaped with their future journey in mind.
In this on-demand session, industry experts walk you through the regulatory landscape of clinical document disclosure and show how to author with compliance, transparency and operational efficiency at the core.
Key Learning Objectives
By watching this session, you’ll learn how to:
- Define and interpret the regulatory requirements that support transparent disclosure of clinical documents.
- Recognize and proactively reduce sensitive or high-risk content through structured, lean and consistent scientific writing.
- Implement cross-functional collaboration and authoring practices that integrate anonymization and technology-enabled disclosure workflows.
Featured Presenters
- Honz Slipka, Senior Transparency Specialist, Clinical Disclosure, Certara
- Zach Weingarden, Director, AI Technology & Applications, TrialAssure
Who Should Watch
This on-demand webinar is ideal for professionals in:
- Clinical writing / medical writing
- Regulatory affairs and submissions
- Disclosure and transparency functions
- Document management and content strategy
- Sponsors, CROs and service providers seeking to strengthen regulatory readiness
Watch Now
Access the full on-demand session at your convenience to ensure your teams are prepared for regulatory disclosure challenges now and as they evolve.
