According to the sources the community is 100% committed to helping you become successful before facing the many challenges of introducing medical devices in the UK market.

The individual needs to make sure that declaration of conformism and mechanical documentation with an applicable conformity assessment process has to be performed by the manufacturing company to obtain the UKCA Marking.

Additionally, the MHRA also requires that an application for registration under this rule must be submitted by a localized unit of the product manufacture or by any UKRP abbreviation of UK Responsible Persons.

Cert 3 Global is a leading provider of UK Responsible Person (UKRP) services. We help medical device manufacturers and distributors appoint a UKRP in accordance with the UK's Medical Devices Regulations (MDR).

Some companies provide a highly affordable FDA 510K and UKCA Marking medical device regulatory solution to producers and exporters of medical equipment all over the world.

UK: With its offices in UK, US and EU, Cert 3 Global has been focused to provide its valued clients involved in medical devices, diagnostics, cosmetics, drugs advisory and support with range of regulatory documentations and cGMP advisory.

All UKCA technical documentation must be meticulously preserved and stored for at least ten years following product introduction in order to be produced for examination when required.