Process and Planning Are Key to Successful EU MDR PMS Compliance

siteadmin April 23, 2023

In spite of continuing delays to implementation deadlines for Medical Devices Regulation (EU) 2017/745 (MDR) and the In-Vitro Diagnostic Medical Devices Regulation (EU) 2017/746 (IVDR), the requirements regarding Post-Market Surveillance (PMS), Post-Market Clinical Follow-up (PMCF),…

Source: www.medtechintelligence.com – Read more