SEHTA, Psephos Biomedica & Mosaic Surgical would like to invite you to attend our EU MDR Software/AI Medical Device CE Marking Workshop.
Why attend
There has been an explosion of new digital health technologies such as mobile health apps and artificial intelligence and software medical devices. To sell software and AI as a medical device in the UK and Europe it must have the CE mark. The EU Medical Device Regulation (MDR) is in its implementation phase and will be fully effective from May 2020. All medical devices including new digital health technologies will need to comply with these new regulations.
This one-day event will provide an overview of the
-Software/AI medical device CE Marking Process, Software Device Classification and Conformity Assessment, Technical File including & Quality Management & Post Market Surveillance & Vigilance and the opportunity to hear from your peers.
Costs to attend: – You will be invoiced separately after registration
SEHTA Members: £240+ VAT per delegate
SEHTA non-members :£280+ VAT per delegate (it’s free to join SEHTA – Please click here)
Special Offer if you book 2 workshops in advance
£430 + VAT SEHTA Members / £510 + VAT SEHTA non-members per delegate
Series 3 workshop is on Technical File on 12th June
For further details and to book, please click here.