Post Market Surveillance under EU MDR 2017/745 Training

Post Market Surveillance (PMS) under the EU Medical Device Regulation (MDR) Training is designed to equip quality and regulatory professionals, medical device manufacturers, and post-market teams with the knowledge and tools to meet these rigorous requirements.

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4.8 ★★★★★ 6 Reviews
EU MDR Post Market Surveillance Medical Devices

Post Market Surveillance (PMS) Practitioner

14hrs
RAPS Certified Course

Post Market Surveillance (PMS) Training is for those looking to master the post market surveillance requirements under the EU MDR 2017/745

4.5 ★★★★★ 6 Reviews
EU MDR Post Market Surveillance Medical Devices

Post Market Surveillance (PMS) Requirements

6hrs
RAPS Certified Course

Post Market Surveillance (PMS) Requirements Training is for those looking to understand the fundamentals of post market surveillance requirements under the EU MDR 2017/745

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Training credentials that you can trust.
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