Eclevar UK are pleased to announce their first webinar in a series around the UKCA mark and the future regulations.
20th July 2022 – 11am BST
This inaugural webinar hosts an exciting discussion between experts from across the sector. We have confirmed panel representatives from BSI, ABHI, BIVDA and FIND. It looks to be an informed and engaging debate!
Amongst them there is a wealth of experience in medical device and IVD regulation, across both the UK and EU market. At this critical moment for the UK we are taking the opportunity to look at the MHRA’s recent consultation response and talk about what that means for the UK MedTech and IVD sector. Expect honest and differing opinions!
We will be looking at what we see as the headlines of the response – what we were pleased to see and what has got us feeling nervous! The panel will be discussing the impact across the sector, from the point of view of industry for both MedTech and IVDs as well as thoughts from an Approved Body.
If you have any questions you would like the panel to answer, please do submit them to Eclevar UK by 19th July 2022.
