For over 20 years, Lucid’s designers have helped clients create award-winning medical devices, wellness, safety and security systems.
In the highly regulated sectors Lucid clients specialise in, achieving a third BSI audited reaccreditation for ISO 13485 medical device design and manufacturing is an essential external validation of the team’s know-how and experience.
Since 2012 Lucid has been certified for medical device design to ISO 13485, the medical device industry’s quality management system (QMS) harmonised standard, and in 2018 achieved certification for medical device manufacturing, too.
Recently Lucid achieved @BSI recertification for both design and manufacture, with zero nonconformities.
For more information on how Lucid help clients design and manufacture medical devices, contact [email protected]
