How long can I continue to supply my medical devices to the UK? That is one of many questions. We have summarized important key points for you.

As of January 01, 2021, the framework conditions regarding the regulation of medical devices in the UK have changed. Medical device manufacturers will have to face new challenges. For example, the introduction of medical devices into the United Kingdom will be subject to a number of changes, including the need for a UK Responsible Person and the introduction of new conformity marks.


* Impact
* Legislation for CE marking
* Transition periods
* UKAS Mark of Conformity
* Registration

Mirjam Ruess

As head of auditor management, Mirjam Ruess is responsible for the maintenance, further education, and expansion of our auditor pool. This includes the acquisition and evaluation of applicants as well as the provision of technical competencies of auditors for the responsible authorities. In addition, Ms. Ruess is deputy managing director and authorized signatory of DQS MED as well as product manager for the ISO 9001 framework.