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
LR offers a range of services to organisations operating within the medical devices industry including:
- Medical Device Regulation (MDR) training courses
- In Vitro Diagnostic Device Regulation (IVDR) training courses
- ISO 13485 accredited certification and training courses
- MDSAP certification and training courses
LR's experts regularly share their research and insights.
Who we work with
We help thousands of organisations, 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.
Helping Terre de Hommes help children globally. Certification to ISO 9001:2015 redesigns the NGO’s operating structure. Read more in our case study.
Our latest updates
Join us at these forthcoming events
4 May 20
Offshore Technology Conference 2020.
12 Jun 20
ISO 45001:2018 Migration Seminar
29 Jun 20
CMA Shipping 2020.