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2010 Biosimilar Prescribing Outlook

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This study - designed, executed and analyzed by research professionals from the drug development and commercialization industry - sheds light on prescribers' views of biosimilars. It is based on interviews with 264 physicians in the United States and Western Europe. Respondents provided their beliefs, attitudes, intentions, and expectations on a number of biosimilar related topics including:

  • Regulatory issues
  • Safety and efficacy
  • Prescribing / Pricing
  • Development / Testing rigor
  • Differences between "generic" and "novel" manufacturers

What Readers Will Learn

Sponsors and service providers can rely on this report to provide an important perspective on their development and commercialization strategies for Biosimilar products.

Other Measurements Reported

  • Adoption of prescribing
  • Anticipated pricing (discount level)
  • Generic vs. innovator manufacturing safety and efficacy

Table Of contents

This report is divided into four major sections

1. Regulatory Awareness

2. Safety and Efficacy

3. Perceptions of Generic and Innovator Companies

4. Prescribing Behavior

As always, an appendix of Charts and Graphs is also included within this report with responses to all questions asked in this study

2010 Biosimilar Prescribing Outlook

Published By: CHI Healthtech
 

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