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Biosimilars in Europe
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This reprint examines regulatory, pricing and reimbursement issues related to the market access and uptake of off-patent biologics, biosimilars, next-generation biologics and competing innovative medicines in European countries.

This book is included in DOAB.

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Keywords

  • adalimumab
  • approval
  • award criteria
  • Barriers
  • Belgium
  • biological
  • biologics
  • biosimilar
  • biosimilar market
  • biosimilar sustainability
  • biosimilar/supply and distribution
  • biosimilarity assessment
  • biosimilars
  • budget impact analysis
  • clinical
  • clinical governance
  • Communication
  • Competition
  • competitive market
  • cost containment
  • cost simulation
  • Delphi technique
  • drug costs
  • Economics, finance, business & management
  • Education
  • etanercept
  • Europe
  • European public assessment reports (EPARs)
  • Germany
  • healthcare costs
  • HER2-positive breast cancer
  • incentives
  • Industry & industrial studies
  • infliximab
  • information
  • interchangeability
  • Intravenous
  • Manufacturing industries
  • market dynamics
  • medicine
  • n/a
  • off-patent
  • Patient
  • Pharmaceutical industries
  • pharmaceutical spending
  • Policies
  • potentially critical quality attributes (pCQAs)
  • Pricing
  • Procurement
  • quality attributes (QAs)
  • queries
  • reference biological
  • Regulatory
  • regulatory science
  • reimbursement
  • review
  • savings
  • Spain
  • subcutaneous
  • sustainability
  • switching
  • tender
  • TNFα inhibitors
  • trastuzumab
  • uptake
  • Utilization

Links

DOI: 10.3390/books978-3-0365-6574-3

Editions

edition cover

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