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UK-RP

UK RP - UK RESPONSABLE PERSON.

The transition period for the UK to leave the European Union ended on December 31, 2020. If you are a manufacturer outside of the UK, you need to designate a UK Responsible Person when producing. your product is placed on the UK market.

Won-Med has signed with CMC a global certification body with extensive experience in services EC Representative has extended our customer support as well as providing the service of the responsible person in the UK. Great Britain.

The responsible person in the UK will perform specific duties on behalf of the manufacturer in relation to the manufacturer's obligations. This includes registering a manufacturer's equipment with the MHRA before it can be placed on the UK Market. The UK responsible person will need to be listed on the product label.

All medical devices, including in vitro diagnostic medical devices, need to be registered on a new basis, however the MHRA has established different renewal periods depending on the product classification.

For more information, please contact us.

CONSULTING - INTERNATIONAL CERTIFICATE

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Tel: +84 (0) 283 620 6200 - Hotline: 0325269326.

Email: [email protected]

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