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 centered around keeping patients safe and protecting their information in a period where technology continues to advance.
LRQA offers a range of services to organizations operating within the medical devices industry including:
- ISO 13485 accredited certification and training courses
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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 maximize 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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