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.
Lloyd’s Register 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?
Trident Medical Services: Setting sector standards as ISO adopters
Setting sector standards as early ISO adopters. Certification to the revised ISO 9001:2015 standard for quality management. Read our case study.
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