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Faster Device Certification Among Keys To Unlocking Innovation In EU MedTech Sector

 
• By Amanda Maxwell

While MedTech Europe sharpens its focus on what the EU most urgently needs to advance the medtech market in four targeted measures, the European Commission has also unveiled four priorities for 2025.

Finding Regulatory Solutions To Rapidly Improve EU Medtech Opportunities (Shutterstock)
Key Takeaways
  • High costs and regulatory unpredictability discourage innovation and investment in the EU and endanger patient access to devices.
  • Improving market access conditions and ways of maintaining products on the market is key.
  • Industry also wants a phasing out of routine recertifications.

How can the EU speed up its medtech certification process in a way that will encourage manufacturers to innovate and launch their products in Europe before other markets?

That is the issue being addressed in a document just released by MedTech Europe — Europe’s largest medical device trade association – outlining four priority measures...

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