NSF Health Sciences

Experts in Medical Device Training, Testing, Consulting, Auditing and Regulatory Support

New EU Medical Device Regulation Adopted

NSF Health Sciences

This year has brought significant changes to the regulatory landscape across Europe, following the publication of the new European medical device regulation (MDR) and in-vitro diagnostics regulation (IVDR).

NSF International hosted an industry forum in the UK on 30 November 2016 to explore the likely impact of changes on company planning, finance, and human resources, particularly in the areas of quality assurance and regulatory / manufacturing functions.

To find out more about the changes of medical device regulation, including implications for IVDs, the pharmaceutical perspective, industry planning for new directives, and future developments, download this free whitepaper.

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