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

Post Market Surveillance (PMS) Practitioner

14hrs
RAPS Certified Course
Price: 1095.00

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 Training

6hrs
RAPS Certified Course
Price: 695.00

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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2026 Training Guide

Transformational Training for ISO Standards, Auditing & Medtech QA/RA

2026 Training Guide

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Our team has you covered with expert insights & updates to stay on top of the latest updates, trends, and changes in the industry.

Reaffirmed, Not Static: ISO 13485 and the Global Regulatory Evolution
Michelle discusses the recent affirmation of ISO 13485:2016 and shares her insights on the new guidance reflecting a Global Regulatory Evolution....
Low Risk Does Not Mean No Risk
Michelle discusses why ISO 13485 and ISO 14971 make a critical clarification on Risk, and clarifies a dangerous misconception in medical device develo...
MDCG Manual on Borderline and Classification (Version 4)
Borderline products remain one of the trickiest challenges under the EU Medical Device Regulation (EU) MDR 2017/745 and the In Vitro Diagnostic Regula...