Join expert presenters; Breda Kearny - Clinical Regulatory Lead, BSI, Diane M. Legere - Senior Clinical Auditor, DNV, Marcus Torr - Head of Post Market Surveys, Purdie Pascoe and Efsthathios Vassiliadis - CEO, Evnia for this insightful live event.
Real world data (RWD) is transforming the way medical devices are developed, evaluated, and improved. This data provides a rich, diverse picture of how devices perform across varied populations and settings. It enables manufacturers to generate real world evidence (RWE) that supports claims of safety and effectiveness, informs regulatory decisions, and drives innovation.
Purdie Pascoe is delighted to host this 60-minute live webinar in which leading experts from across the industry are uniting together to provide you with key considerations to help improve your RWD collection for regulatory approvals.
Key takeaways
Notified Body perspectives: Gain consolidated regulatory insights into the use of RWD from two renowned Notified Bodies – BSI and DNV
Device lifecycle management: Key considerations including real-world examples to help your RWD planning
Post Market Surveys for data collection: Understand why Post Market Surveys are a powerful tool in collecting RWD
Live Q&A: Submit your questions upon registering and during the live event
Ready to take your RWD strategy to the next level?
Don’t miss this opportunity to gain practical, insider insights from leading experts.
Purdie Pascoe Post Market Surveys expertise
With over 500 surveys conducted in the past five years, we’ve built unmatched expertise across device types and risk classifications.
Whether you need full-service support or help at specific stages, our team ensures you collect the clinical / real world data you need to remain proactive and compliant across global regulations. This focus has earned us the trust of manufacturers worldwide, strong partnerships with notified bodies and continuous repeat business.