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DTSTART;TZID=Europe/London:20190424T103000
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DTSTAMP:20260412T204945
CREATED:20190318T114829Z
LAST-MODIFIED:20190318T114829Z
UID:17949-1556101800-1556121600@staging.medilinkmidlands.com
SUMMARY:EU MDR Software/Al Medical Device CE Marking Workshop
DESCRIPTION:SEHTA\, Psephos Biomedica & Mosaic Surgical would like to invite you to attend our EU MDR Software/AI Medical Device CE Marking Workshop. \nWhy attend \nThere 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. \nThis one-day event will provide an overview of the \n-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. \nCosts to attend: – You will be invoiced separately after registration \nSEHTA Members: £240+ VAT per delegate \nSEHTA non-members :£280+ VAT per delegate (it’s free to join SEHTA – Please click here) \nSpecial Offer if you book 2 workshops in advance \n£430 + VAT SEHTA Members / £510 + VAT SEHTA non-members per delegate \nSeries 3 workshop is on Technical File on 12th June \nFor further details and to book\, please click here.
URL:https://staging.medilinkmidlands.com/event/eu-mdr-softward-al-medical-device-ce-marking-workshop/
LOCATION:Hempsons\, 100 Wood Street\, London\, EC2V 7AN\, United Kingdom
ORGANIZER;CN="SEHTA":MAILTO:info@sehta.co.uk
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