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SUMMARY:EU Medical Device Technical Files Workshop
DESCRIPTION:SEHTA\, Psephos Biomedica & Mosaic Surgical would like to invite you to attend our EU Medical Device Technical Files Workshop. \nWhy attend \nThe new EU Medical Device Regulation (MDR) is in its implementation phase and will be effective from May 2020. All medical devices will need to comply with this new legislation. Similarly\, the IVD Regulation (IVDR) will be in force from May 2022. Many companies are not yet ready for the journey let alone have a roadmap of how to get to compliance. \nThis one-day event will: \nProvide you with an overview of the key requirements for technical documentation in order to comply with the MDR and your conformity assessment\nAssist you in assessing your company’s current preparedness for the transition\nProvide a clear\, practical guide to the next steps that you and your company need to take to meet Technical documentation requirements to gain CE Marking under the MDR \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 2 workshop is on Software/AI Medical Device CE Marking on 24 April \nFor full details and to book your place\, please click here.
URL:https://staging.medilinkmidlands.com/event/6059/
LOCATION:Hempsons\, 100 Wood Street\, London\, EC2V 7AN\, United Kingdom
CATEGORIES:Medilink Partner Event
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