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Key EU and US regulatory changes on the horizon that impact the medical device and IVD sectors

 

Medtech webinar



Find out how the industry is likely to change in the coming months/years. Listen to top speakers Amanda Maxwell, Regulatory Affairs Editor and David Filmore, Executive Editor from the Pharma Intelligence team talk about:


  • US regulatory market overview, including a look at the shift in focus of the FDA as well as improvements made in their efficiency
  • Key points of evolution to expect in the US; exploring real-world data and its uses, nascent regulatory mechanisms and changes in IVDs
  • User fee reauthorization and key outputs
  • EU regulatory overview, including current directives, new regulations for devices and IVDs and the key regulatory players
  • Key EU regulatory changes and how manufacturers must prepare, across medical device regulation and IVD regulation
  • Dalli Plan of Joint Actions
  • An update on the UK and Brexit

 

Register here today!