It may not have made many headlines, but when the new Medical Device Regulation (MDR) came into force on 26th May this year, it brought with it important implications for all economic operators in the medical device supply chain in Europe, including home oxygen service providers.
While it doesn’t change the status of home oxygen service providers from the existing Medical Device Directive (MDD), the MDR does strengthen regulations and brings much needed clarity to their role, responsibilities and liabilities.
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