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. Join this interactive workshop to find out more about the key areas of change within the MDR and IVD regulations.
Date: 5 February 2019
Location: Medilink West Midlands, 4 Greenfield Crescent, Edgbaston, Birmingham B15 3BE
Times: 10:00 - 16:15
Cost: Medilink members fee: £180 + VAT/ Medilink non-members fee – £215 + VAT per delegate