Accelerating Regulatory Submissions: Practical AI Workflows for MDR and IVDR Compliance

Webinar on Accelerating Regulatory Submissions: Practical AI Workflows for MDR and IVDR Compliance

Tuesday, November 11 at 11am ET

How are medical device and diagnostic manufacturers meeting evolving regulatory standards through AI-enabled systematic literature review workflows? Explore this topic with the experts and gain real-world insights for enhancing transparency, traceability, and speed across regulatory submissions.

As regulatory expectations for evidence continue to evolve, frameworks like MDR and IVDR are setting new standards for compliance across the healthcare landscape.

Join Sue Lacey Bryant, former Chief Knowledge Officer for England’s National Health Service (NHS), Dr. Rhodri Saunders, Founding Director of Coreva Scientific, and Eitan Agai, Founder of PICO Portal, for an expert-led session on practical, AI-assisted approaches to regulatory-grade literature reviews.

You’ll see how SLR platforms, like PICO Portal, can help streamline evidence generation – cutting review cycle times, improving audit readiness, and maintaining “living” updates aligned with MDR and IVDR requirements.

What You’ll Learn

• How to plan, execute, and maintain regulatory-grade literature reviews with automation and AI
• Best practices for ensuring traceability and audit readiness
• Ways to reduce review cycle times while maintaining compliance
• Insights from NHS and Coreva Scientific leaders on modernizing evidence workflows

Date and Time:

Tuesday, November 11th, 2025
11 am – 12 pm Eastern Time (New York) / 4:00pm GMT (United Kingdom)

Can’t make it live? Register to receive the recording.