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Webinar // UKCA Requirements for Medical Device Manufacturers

⇓ Open me ⇓.

Complying with the UK’s leave from the European Union (EU), the needs for clinical tools is outlined in regulations, the Medical Devices Regulations 2002 (SI 2002 No 618, as changed) (UK MDR). The UK MDR covers the regulations for tools being put on the marketplace in the UK (Great Britain, GB as well as Northern Ireland, NI).