Expert Opinion Panels and New Guidance Documents Are Part of the Changing Landscape of MDR 2017/745
Author: Suzanne Broussard, PhD | February 25, 2022 The European Union (EU) saw 2021 bring important milestones and changes to the implementation of Medical Device Regulation (MDR) 2017/745. Key highlights […]
[Ask the Expert] Safety and Performance (MDR)
This session’s topic: Safety and Performance Measures and Acceptance Criteria for MDR Do you have questions about how to identify meaningful safety and performance measures for the clinical evaluation? What […]
[FREE WEBINAR] Post-Market Literature Surveillance: Systematic Literature Review and Case Study
Click here to watch the webinar Key Takeaways: How leveraging published data can help meet regulatory expectations and inform internal decision-making Steps for conducting a methodologically-sound SLR How data obtained […]
