This one-day event will:-

  • Provide you with an overview of the key areas likely to need upgrading to comply with the MDR/IVDR
  • Assist you in assessing your company’s current preparedness for the transition
  • Give you a clear, practical guide to the next steps that you and your company need to take to gain CE Marking under the MDR/IVDR

Outcomes

  • Gain an overview of the new EU Medical Device and IVD Regulations
  • 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

Click here to view the event agenda


Target Companies:

Medical Device & IVD companies as well as those 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 and IVD 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.