Stringent requirements require an experienced partner.
The complex healthcare and medical landscape is adapting and changing constantly. The welcome introduction of new medical device regulations indicates one of the most significant developments within medical device manufacturing for a number of years. While this aims to address some medical device related issues, the sector as a whole faces several other significant challenges, many of which are centred around keeping patients safe and protecting their information in a period where technology continues to advance.
At Lloyd's Register (LR), we recognise that every organisation and its processes are unique. As a leading notified body for over 20 years we also understand the impact and importance of effective regulatory compliance and the need to fully understand the specific circumstances of our clients and their businesses.
How we can help
We apply our expert solutions and independence to assure the integrity, reliability and success of every aspect of your operation. Helping maximise productivity and recovery, reduce operating costs, mitigate risk and demonstrate compliance with government regulations, industry codes and standards, many of which we have helped to develop.
LR's experts regularly share their research and insights.
Who we work with
We help businesses across dozens of sectors push forward and achieve like never before. How can we help you?
Our latest updates
US FDA announces plans to use ISO 13485 for medical devices regulation
LR achieves global accreditation for 'Parts & Services' for ISO 13485:2016
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15 Nov 18
Cyber Security Summit & Expo
London, United Kingdom