|Articles|June 15, 2003

BioPharm International

  • BioPharm International-06-01-2003
  • Volume 16
  • Issue 6

Inside Washington: Reshaping Biotech Drug Development

Author(s)Jill Wechsler

by Jill Wechsler, BioPharm International FDA is examining policy options for incorporating genomic information into the regulatory process while encouraging manufacturers to share pharmacogenomic research.
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Guest Interview: A Strong Dose of Reality: Visiting with Cynthia Robbins-Roth

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Collaborating Across the Extended Pharmaceutical Enterprise: How Sharing Information Leads to Process Enablement

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Sialylation Levels Influence Oligosaccharide Quantitation: Analyzing Response Variability Using High-pH Anion-Exchange Chromatography and Pulsed Amperometric Detection

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SOX in the Boardroom: What the Sarbanes?Oxley Act Means to You

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The Project Management Institute's Pharmaceutical Specific Interest Group 2002 Benchmark Survey Results: Project Managers and Project Management in the Biotech Industry

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Small Biopharms Face Unique Challenges: Outsourcing in Early-Stage Drug Development

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BioTrends: M&A Malaise

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