UL Achieves Transition Accreditation For The 2016 Version Of ISO 13485

Medical device customers can now receive audits and certificates to ISO 13485:2016 to align with global regulatory requirements.

FREMONT, California, March 30, 2017 /PRNewswire/ -- UL (Underwriters Laboratories), a global safety science organization, announced today it has successfully completed its assessment and received accreditation by the Standards Council of Canada (SCC) as a registrar under the latest version of the quality management system standard for medical devices, ISO 13485:2016 and ISO 13485:2016 under CMDCAS.

Regulators around the world use ISO 13485 as a base standard as part of their regional requirements to address medical device quality management systems.  The 2016 version is the first revision in over 10 years, as it replaces the 2003 version implemented by over 26,000 manufacturing sites worldwideⁱ.  The major changes include more emphasis on taking a risk based approach, better controls over suppliers and verification processes for connected devices. 

"UL is committed to making sure our medical Quality System Registration customers are able to demonstrate compliance with the latest standards and current requirements," said Michael Windler, Regulatory Service Operations Head for the UL Health Sciences division. 

UL will work together with current and new customers to assess the opportunity to upgrade their certification.  All new ISO 13485 customers will automatically be certified under ISO 13485:2016. With the SCC accreditation, UL qualified staff can begin to audit to ISO 13485:2016 and issue certificates.

ISO 13485 concepts are part of most Regulatory QMS requirements, including the new Medical Device Single Audit Program (MDSAP) for which UL is an Authorized Auditing Organization (AO). 

SCC accredited certificates to ISO 13485:2003 will remain valid until the end of February 2019. Regulatory bodies that recognize a national version of ISO 13485 as part of their regulatory requirements will each define their own transition schedule.

For more information on UL's regulatory certification services, contact us at [e-mail] or visit www.ul.com/medical.

About UL
UL fosters safe living and working conditions for people everywhere through the application of science to solve safety, security and sustainability challenges. The UL Mark engenders trust enabling the safe adoption of innovative new products and technologies. Everyone at UL shares a passion to make the world a safer place. We test, inspect, audit, certify, validate, verify and train and we support these efforts impartially with software solutions for safety and sustainability. To learn more about us, visit UL.com.

ⁱ ISO Survey of Management System Standard Certifications 2015 https://www.iso.org/files/live/sites/isoorg/files/standards/conformity_assessment/certification/doc/survey_executive-summary.pdf

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