Implement a framework for high-quality medical devices.
The medical device industry is entering its most significant period of regulatory change since the 1990s. While the new regulatory landscape will bring complex challenges for manufacturers, it will also introduce essential changes designed to enhance patient safety and enable the introduction of more innovative medical device solutions.
Our range of medical services
LRQA offers a range of services to organizations operating within the medical devices industry including:
- ISO 13485 accredited certification and training courses
LRQA's experts regularly share their research and insights.
Who we work with
We help thousands of organizations, from the world's best known brands to the smallest of suppliers. How can we help you?
Helping NGO, Terre de Hommes, help children globally.
Learn how achieving ISO 9001:2015 certification redesigned the NGO's operating structure, so they can help more children globally.