¹û¶³Ó°Ôº

The purpose of the consultation is to develop a future regime for medical devices which enables:
•ÌýÌý ÌýImproved patient and public safety;
•ÌýÌý ÌýGreater transparency of regulatory decision making and medical device information;
•ÌýÌý ÌýClose alignment with international best practice, and;
•ÌýÌý ÌýMore flexible, responsive and proportionate regulation of medical devices.

The MHRA welcome the views of patients, medical device researchers, developers, manufacturers and suppliers, clinicians, other healthcare professionals and the wider public to help shape future approach to regulating medical devices in the UK.
¹û¶³Ó°Ôº Institute of Healthcare Engineering is responding to this consultation in two ways.Ìý

1. Encourage ¹û¶³Ó°Ôº staff with vested interest in medical devices regulations to submit a personal response to the call by completing the MHRA online survey .ÌýThis online survey closes on Ìý25 November 2021 at 11:45pm.
2. IHE will be submitting an institutional response and we are inviting colleagues to share with us any specific views and concerns that they feel should receive institutional representation. To submit your views please complete this . Comments will be collated until 25th October 2021.

If you have any questions or would like further information, please contact marilyn.aviles@ucl.ac.uk (IHE R&D Manager)Ìý
Ìý