LRQA Global Medical Devices Survey 2016

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Be a part of the inaugural LRQA Global Medical Devices Survey, where we poll experienced regulatory affairs professionals worldwide on the future of the medical device regulations.

Medical Devices Regulation (MDR)

Medical Devices Regulation (MDR)

What can you do about the new MDR before it gets published in Q4 2016?

In Vitro Diagnostic Device Regulation (IVDR)

In Vitro Diagnostic Device Regulation (IVDR)

Find out if you are ready for the new IVDR

ISO 13485:2016 Certification

ISO 13485:2016

Your company could benefit from our ISO 13485:2016 services

In Vitro Diagnostic Device Regulation (IVDR)

Medical Device Single Audit Program (MDSAP) Certification

Certified once, recognised globally. Is the MDSAP for you?