PMS Archives - Medical Innovation Exchange

Process and Planning Are Key to Successful EU MDR PMS Compliance

Leave a Comment / EU MDR/IVDR, Focus Article, literature review, Medical Device, MedTech, nonconformances, off-label, PMCF, PMPF, PMS, poat market surveillance, PRRC, Quality/Regulatory, RC - EU MDR and IVDR, RC - Medtech Regulatory Resource Center / By Inga Hansen

Process and Planning Are Key to Successful EU MDR PMS Compliance 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), Post-Market Performance Follow-up (PMPF), and Person Responsible for …

Process and Planning Are Key to Successful EU MDR PMS Compliance Read More »

MedTech Regulatory Compliance: Join the Discussion and Expand Your Regulatory Networks

Leave a Comment / case for quality, cybersecruity, From The Editor's Desk, ISo 13845, Medical Device, MedTech, PMS, premarket approval, Quality/Regulatory, RC - Medical Recall, recalls, regulatory compliance, remote inspections / By Inga Hansen

MedTech Regulatory Compliance: Join the Discussion and Expand Your Regulatory Networks From cybsecurity to remote inspections, recalls and quality management, medical technology regulations are rapidly expanding. This increase in global regulatory demands has presented new challenges for regulatory affairs and intelligence teams. On May 16-17, The MedTech Regulatory Intelligence Summit will bring together regulatory …

MedTech Regulatory Compliance: Join the Discussion and Expand Your Regulatory Networks Read More »

MedLance

E-Learning

Moderators

PMS

Process and Planning Are Key to Successful EU MDR PMS Compliance

MedTech Regulatory Compliance: Join the Discussion and Expand Your Regulatory Networks

Quick links

MedTech Minds

FDA Courses

Forum
News

About

Contact

Newsletter

Quick Links