New EU MDR guidance on responsibilities of importers and distributors

December 10, 2021
Edmund Proffitt

The European Commission's Medical Device Coordination Group (MDCG) has published a guidance document containing questions and answers on the roles of importer and distributor under the EU MDR.

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New EU MDR guidance on responsibilities of importers and distributors

More To Explore

Call for input into Government’s 10 Year Health Plan, DHSC launches ‘Design for Life’ medtech roadmap

Attitudes to Artificial Intelligence in dentistry – BDIA Technology & Trends Survey 2024

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