This one-day workshop will give you:
An overview of the new EU Medical Device CE Marking Process
Help you to maintain Access to the Market
Understand the key areas of compliance required
Understand the technical documentation that should be in place for each device
Gain a plan of action for implementation and CE Marking under the new legislation
Target 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.
Please note this is for Medical Device firms only – not Pharma or IVD
Cost: £250 + VAT per delegate – SEHTA Members / £300 + VAT per delegate – Non-Members
The 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.
For further information and to book a place please click here.