BIVDA are in the process of formulating our response to the ongoing MHRA consultation on the new Regulatory framework for medical devices and IVDs in the UK.
This will ultimately be channelled through the UKCA Working Group (initially created as an extension of the Regulatory Affairs Working Party). We fully appreciate that there may be a number of members who are not already a part of this Group who would like to be involved in creating the BIVDA feedback on this consultation, so if you would like to be involved, please contact Ashleigh Batchen (firstname.lastname@example.org) or Stuart Angell (email@example.com) to join.
I would like to emphasise that any BIVDA member can join this group, regardless of the discipline they work in. The only requirement is that you are interested in being involved with the ongoing work relating to this consultation.
Please note that you may not have the opportunity to feed into this consultation response unless you join the UKCA Working Group.
We strongly encourage each organisation to submit your own individual response alongside any BIVDA response. We intend to provide members with the full BIVDA response upon submission.