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SUMMARY:EU MDR Clinical Strategy & Evidence Requirements CE Marking Workshop
DESCRIPTION:This one-day workshop will give you: \nAn overview of the new EU Medical Device CE Marking Process\nHelp you to maintain Access to the Market\nUnderstand the key areas of compliance required\nUnderstand the technical documentation that should be in place for each device\nGain a plan of action for implementation and CE Marking under the new legislation \nTarget Market: C suite\, executives\, product owners\, medical officers\, regulatory and clinical specialists within a company that need to understand the overall clinical requirements for their medical devices to enable them to place a device on the market and to maintain access. All company sizes will find it useful. \nPlease note this is for Medical Device firms only – not Pharma or IVD \nCost:  £250  + VAT per delegate – SEHTA Members  / £300 + VAT per delegate – Non-Members \nThe organisers reserve the right to decline registrations based on review. All applicants will be notified by email if they have been accepted for a place no later than Friday 27th September. \nFor further information and to book a place please click here. \n 
URL:https://staging.medilinkmidlands.com/event/eu-mdr-clinical-strategy-evidence-requirements-ce-marking-workshop/
LOCATION:Hill Dickinson\, Broadgate Tower\, 20 Primrose Street\, London\, EC2A 2EW
CATEGORIES:Other Event
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