MPD Impact and Assessment of the new European In Vitro Diagnostic Regulations

29 June 2017 4 Greenfield Crescent, Edgbaston, Birmingham B15 3BE

Medilink West Midlands, in conjunction with Acclaim Biomedical Consulting, is offering a one day workshop exploring the new European Regulations for In Vitro Diagnostics. For the in-vitro diagnostic sector, these new regulations will bring about major shifts in areas such as classifaction, performance evaluation and clinical evidence. The new regulations will be fully applicable in five years. 

Within the IVD sector, expect changes to:

  • The classification system
  • Oversight of the Notified Bodies
  • Performance evaluation
  • Clinical data and trials.

This course will cover all of these key elements, plus more. You will learn about key timelines that you need to be working to and what steps need to be taken next. From this workshop you will take away a specially made checklist which will assist you with making sure that your organisation is working in line with the new regulations

The course is designed for business leaders with a good working knowledge of the current regulatory requirements

You can learn more and book your place on the Medilink West Midlands website. For more information regarding the course and booking, please contact Vanessa Bailey on vanessab@medilinkwm.co.uk or 0121 452 5630.