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Dec 2, 2020
  • Webinar

EU Medical Device Regulation (EU MDR): A Practical Approach

Learn effective and practical approaches that meet EU medical device regulation (MDR) requirements, and how to update them based on notified body feedback.

Close-up of an electrocardiogram monitor in a hospital room

Date & Time

Starts

Dec 2, 2020 1:00pm EST

Ends

2:00pm EST

Location

Onliine webinar

Section of 10.4.1 of the EU Medical Device Regulation (EU MDR) requires identification of carcinogens, mutagens and reproductive toxins (CMRs) and endocrine-disrupting chemicals (EDCs) over 0.1% w/w in invasive, or fluid or gas contacting materials. There is no one standard format for the output requirements. 

This webinar will discuss effective and practical approaches that meet the requirements of EU MDR, and how to update them based on notified body feedback. 

This webinar will explain:

  • What are CMRs and EDCs?
  • What CMRs and EDCs are in medical devices?
  • How to identify CMRs and EDCs in medical devices
Hospital operating room with monitors and equipment

Medtech

Healthcare technology and medical devices are constantly evolving to improve accuracy, patient safety and patient wellness. This rapid progress also leaves these devices increasingly susceptible to quality, safety and cybersecurity issues. We offer safety and compliance testing and training to take on these, and many other issues facing the healthcare device industry.

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