Inside Washington: Reshaping Biotech Drug Development

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

over 22 years ago

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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

over 22 years ago

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BioTrends: M&A Malaise

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Inside Washington: Reshaping Biotech Drug Development

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