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Companion diagnostics are poised to be a huge growth area worldwide, with a CAGR of 20.1% over the next 5 years, making it a $6B industry by 2022. These often in-vitro medical devices provide essential information for the efficacy of a corresponding drug or biological product, and are also used for pre-determining the efficacy of treatment. Their growth is being propelled in most countries by a number of favorable factors

In this recording we focus on the area of oncology technologies and pathways. We discuss:

  • Examples of how companies used these new technology regulations in applications
  • Biomarker-driven drug development
  • Lessons from orphan drug development
  • New technologies in play such as next-gen sequencing and liquid biopsy
  • The regulatory context for these developments






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