Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Accept all cookies Reject all non-essential cookies Find out more

Oxford Medical CE Marking Forum (OxMCEF)

Logo

Join our LinkedIn Group to receive the latest news and updates.

Register for the upcoming Seminars:

February 2018

March 2018

Oxford Medical CE marking Forum aims to to serve as a knowledge exchange portal for interested academic and industry partners within Oxford.

Slides presenting the vision of the Oxford Medical CE marking Forum.
Slides presenting the vision of the Oxford Medical CE marking Forum.

The CE mark signifies the products sold in the European Economic Area have been assessed to meet high safety, health, and environmental protection requirements. The mark is the medical device manufacturer's claim that a product meets the essential requirements of all relevant European Medical Device Directives.

This is a joint initiative in collaboration with Dr Jeroen Bergmann at the Institute of Biomedical Engineering (IBME), MPLS Division.

We are supported by the Medical Sciences Division with an Expert in Residence Scheme, and will be hosting Dr Toni Day (Director of Quality and Regulatory Affairs, OrganOx) for 1-2-1 sessions with researchers who require an initial consultation to scope out the regulatory requirements for their project.

NDS Lead

Related research themes

Safety and Quality
Safety and Quality