Generating high-quality literature reviews is a non-negotiable requirement for EU MDR regulatory submissions. However, the process is often manual, costly, and siloed, leading to duplicated work, inconsistent evidence quality, and slower time-to-market.
This hands-on webinar will demonstrate how Agentic AI can configure and populate DistillerSR clinical evaluation report (CER) templates to integrate third-party adverse event data from Maude and Faeres, transforming the way your organization configures regulatory evidence for CERs and periodic safety update reports (PSURs).

Key Webinar Takeaways

• Rapid Efficiency Gains: Learn how organizations can configure their CER templates using Agentic AI and achieve up to 70% faster completion of evidence screening and data capture for regulatory submissions.
• Accelerated Compliance & Time-to-Revenue: Discover how Agentic AI-enabled workflows accelerate project configuration, time to insight, and time to market by providing instant access to validated, traceable evidence for decision-making and drafting regulatory documentation.
• Mitigate Risk with Trusted Evidence: Understand how Agentic AI grounds all generated reports, summaries, and insights in expertly validated, peer-reviewed literature. This ensures the highest standards of reliability, reproducibility, and traceability—essential for auditable CERs and post-market surveillance.
• Integrate Evidence: See how centralizing evidence and applying Agentic AI and API integration can pull third-party data sources into your DistillerSR project to strengthen your submissions.

Join us on February 19 at 11 am EST and go beyond manual processes and implement a strategy that drives faster, more confident, and more compliant CER submissions.