This is a paid press release. Contact the press release distributor directly with any inquiries.

Claigan Webinar - A Practical Walkthrough of an EU MDR Justification Document

CNW Group

Wed, February 18, 2026 at 4:22 AM GMT+9 2 min read

With detailed examples

OTTAWA, ON, Feb. 17, 2026 /CNW/ - 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:

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

Note - due to the expected demand, there will be two (2) webinars scheduled on February 26th.

**Webinars - Walkthrough of an EU MDR Justification Document

**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.

Cision

View original content:https://www.prnewswire.com/news-releases/claigan-webinar---a-practical-walkthrough-of-an-eu-mdr-justification-document-302689856.html

Cision

View original content: http://www.newswire.ca/en/releases/archive/February2026/17/c0142.html

Terms and Privacy Policy

Privacy Dashboard

More Info