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PAREXEL's Bio/Pharma R&D Statistical Sourcebook

2009 / 2010

Publication Date July 2009
Publisher Barnett International
Product Type Reference Manual
Pages 400
ISBN Number not applicable
Product Code BAR00008
Buy this product or for assistance call +44 20 7060 7474

Summary

Now industry's most widely read reference on emerging pharma/biotech R&D trends worldwide, PAREXEL's Pharmaceutical R&D Statistical Sourcebook 2009/2010 features hundreds of all-new, real-world studies, analyses, articles, and data sets providing fresh insights into the developments reshaping pharma R&D and the industry itself.

  • New proprietary analyses on US clinical trial starts, now segmented for the first time by therapeutic category, as well as overall active clinical trials, also segmented by therapeutic category. See how quickly the numbers of active clinical trials are growing, and precisely which therapeutic areas are driving this growth.

  • An all-new and comprehensive analysis of clinical research offshoring in which we provide the first definitive analysis of the countries in which pharma companies are now locating their new clinical trials (based on new studies initiated in 2006). The results will surprise you.

Supported by thousands of graphs, illustrations, and analyses, PAREXEL'S Pharmaceutical R&D Statistical Sourcebook 2009/2010 provides the latest intelligence on every aspect of pharmaceutical development--from product discovery to R&D performance and productivity to time-to-market trends.

An invaluable resource for executives and managers working within or with the pharma and biotech industries, this 2009/2010 compendium puts real-world data sets at your fingertips for presentations, reports, business development efforts, meetings, and critical decision-making analyses:

  • New R&D Spending Trends (U.S. and Global)
  • International Statistics on Drug Development Output Industry-wide and Company-by-Company
  • Emerging Data on the Worldwide and Company-specific R&D Pipelines and Product Launch Trends
  • New Analyses on Drug Development Costs/Development Cycle Times/Attrition Rates
  • Drug Approval Statistics Compiled from FDA, EMEA and other Key Regulatory Agencies
  • International R&D Data from Key Global Markets
And in response to customer demand, the new 2009/2010 edition is once again available in electronic format. Gain instant access to the data, analyses, and benchmark provided in the hardcopy compendium on a fully searchable, hyperlinked and printable web-based edition!

From an in-depth an analysis on the realities of migrating clinical trials to developing nations to advances in clinical trial simulation and genomics to emerging trends in industry's product pipeline and product success rates to the new demographics of US clinical investigators and clinical trial populations, make sure that your meetings, reports, presentations, and decision-making are based on the very best and latest data available today!

Delivery Details

PRINT/CD-ROM:Despatched within 1 to 2 working days.