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 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
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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.
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We help businesses across dozens of sectors push forward and achieve like never before. How can we help you?
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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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