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Signatera for detecting molecular residual disease from solid tumour cancers

  • Medtech innovation briefing
  • Reference number: MIB307
  • Published:  04 October 2022

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  • Overview
  • Summary
  • The technology
  • Regulatory information
  • Equality considerations
  • Clinical and technical evidence
  • Expert comments
  • Expert commentators
  • Development of this briefing

Regulatory information

Signatera is a CE-marked class IVD General in vitro diagnostic medical device under the EU In Vitro Diagnostic Medical Devices Directive (IVDD).


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