Login / Signup

Opportunities and Risks of UK Medical Device Reform.

Ji Eun Diana HanHussein IbrahimOlalekan Lee AiyegbusiXiaoxuan LiuEliot MarstonAlastair K DennistonMelanie Jane Calvert
Published in: Therapeutic innovation & regulatory science (2022)
The UK's medical device sector is at a time-critical juncture to construct a regulatory framework to navigate its exit of Europe and respond to Europe's transition to new medical device regulations whilst also addressing the ongoing demand for rapid approval for new devices in response to the global pandemic. Investment, capacity-building, and international engagement will play a central role in mitigating risks and maximizing opportunities for medical device regulation.
Keyphrases
  • healthcare
  • sars cov
  • coronavirus disease
  • human health
  • transcription factor
  • risk assessment