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
Advanced Oncotherapy PLC shares rise following ISO 13485 certification
US FDA announces plans to use ISO 13485 for medical devices regulation
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7 Oct 20
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CMA Shipping 2020.