Medical devices in the wild: Tracking real world data for lasting impact
Notified Body insights, lifecycle management & collecting data with Post Market Surveys
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.
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.
Watch the webcast in which leading experts from across the industry united together to provide you with key considerations to help improve your RWD collection for regulatory approvals.
Complete the form below to watch the webcast:
Privacy Note: At Purdie Pascoe, we occasionally share the latest MedTech news and insights that we believe may be of interest to you. We will only contact you about topics relevant to your preferences. Your privacy is important to us — you can unsubscribe from our communications at any time. For more information, please see our Privacy Policy.