Elegant Uk Responsible Person Agreement Template. Web activ supported experts in medical device regulatory service, uk responsible person service, etc. Use get form or simply click on the template preview to open it in the editor.
Get emails about this page. Applies to england, scotland and wales. Streamline your compliance journey with us.
Web the uk has updated its guidance on the uk responsible person. Get emails about this page. Web activ supported experts in medical device regulatory service, uk responsible person service, etc.
Legislation that applies in great britain. Applies to england, scotland and wales. Web upon quote acceptance we will set up the ukrp appointment agreement and help you prepare a letter of designation to appoint us a your uk responsible person and.
Web medical devices are one of, if not the most, complicated, and tightly regulated products to place on the market within the european union and the united. In addition, under the uk mdr 2002, technical documentations must be provided to your uk. An overview of the top 10 questions regarding the uk responsible person & medical device and ivd registration with the mhra.
Until that date, we have a grace period and the eu ce mark will be accepted. Web there will be new regulation in the uk, ukca, which will be mandatory by june 2023. Medicinal products sourced from northern ireland for wholesale purposes are out of scope of this guidance.
Web this uk responsible person agreement should be in the form of a headed letter or a signed contract which states the company name and address for both the overseas. Web the mhra will only accept registration of devices from manufacturers or uk responsible persons that are based in the uk, or from authorised representatives. A mutually signed agreement between the legal manufacturer and the uk.
