SEHTA Members: £240+ VAT per delegate
SEHTA non-members :£280+ VAT per delegate (it's free to join SEHTA – Please click here)
The 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.
This one-day event will:
Target Companies: Medical Device companies and Pharma companies with combination products.
Target Market: C-suite, executives, product owners, medical officers, regulatory and clinical specialists within a company that need to understand the overall requirements of the new Medical Device Regulation for their medical devices to enable them to place a device on the market and to maintain access after May 2020. All company sizes will find it useful, but particularly helpful for smaller, resource constrained organisations.