With detailed examples
OTTAWA, ON, Feb. 17, 2026 /PRNewswire/ – On February 26th, Claigan will be hosting a walkthrough of all the elements of an EU MDR Justification Document. This webinar will be the most tangible walkthrough of a Justification Document for CMRs under the EU Medical Device Regulation (MDR). Claigan’s webinar will go over what has to be covered in each section (and when you should start!) and will use a dozen examples of medical devices examples.
If a medical device has a carcinogen, mutagen, or reproductive toxin (CMR) in an invasive situation, fluid path, or gas path it has to be labelled and justified under section 10.4 of the EU Medical Device Regulation (EU MDR).
With the addition of cobalt and NMP to the CMR list, the majority of invasive, fluid, or gas path medical devices are now requiring justification documents for compliance to EU MDR.
Example affected products include needles, trocars, catheters, vision systems, ventilators, endoscopes, glucose monitoring systems, stents, and dental files.
Key topics will include:
Date: 26 February, 2026
Time: 10am and 2pm
Duration: 1 hour including Q&A
To Register:
10am – https://us06web.zoom.us/webinar/register/WN_1WIRbMtKScyx53mtgna1zA
2pm – https://us06web.zoom.us/webinar/register/WN_MQDVtov2TQatNAachK-HYg or on Claigan’s Website at www.claigan.com/webinars About Claigan Environmental (www.claigan.com) Claigan is the leading provider in restricted materials compliance (consulting and testing). Claigan has tested thousands of products for EU MDR, PFAS, Section 71, REACH, POP, TSCA, Prop 65, and related global compliance. Claigan is an ISO 17025 accredited laboratory, expert consultancy, and is dedicated to providing practical solutions for supply chain due diligence and social responsibility. At Claigan, our philosophy is simple: More Results, Less Journey. SOURCE Claigan Environmental Inc.
- Why cobalt and NMP are so common in medical devices
- Description and characterization
- Use and function
- Assessment of risks
- Assessment of possible and relevant alternatives
- Comparison of functionality, performance, risk, and benefits
- Timelines and deadlines
Date: 26 February, 2026
Time: 10am and 2pm
Duration: 1 hour including Q&A
To Register:
10am – https://us06web.zoom.us/webinar/register/WN_1WIRbMtKScyx53mtgna1zA
2pm – https://us06web.zoom.us/webinar/register/WN_MQDVtov2TQatNAachK-HYg or on Claigan’s Website at www.claigan.com/webinars About Claigan Environmental (www.claigan.com) Claigan is the leading provider in restricted materials compliance (consulting and testing). Claigan has tested thousands of products for EU MDR, PFAS, Section 71, REACH, POP, TSCA, Prop 65, and related global compliance. Claigan is an ISO 17025 accredited laboratory, expert consultancy, and is dedicated to providing practical solutions for supply chain due diligence and social responsibility. At Claigan, our philosophy is simple: More Results, Less Journey. SOURCE Claigan Environmental Inc.
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