BIVDA’s Regulatory Affairs Manager Ashleigh Batchen is to join a webinar based on the UKCA Mark and other regulatory topics of note to life science companies on 20 July.
This inaugural webinar hosts an exciting discussion between experts from across the sector. Eclevar have confirmed panel representatives from BSI, ABHI, BIVDA and FIND.
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, the panel 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.
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.
Please find more info on the event here.
