Stringent requirements need 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.
Lloyd’s Register offers a range of services to organisations operating within the medical industry including:
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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.
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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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