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Global Supply Chain Management for Drugmakers
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FDA Cites Generics Maker Heritage Over Postmarket Reporting Woes
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EMA Prepares to Overhaul EudraVigilance Online Adverse Event Reporting Program
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More Compounders Face Off With the FDA
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FDA Orders Drug Interaction Studies on Potassium-Lowering Kayexalate
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U.S. FDA’s Tropical Disease Priority Review Voucher Fee Set at $2.7 Million
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ICH Advises on Acceptable Exposure for 15 Carcinogens
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House Panel Looking Into Blood Thinner’s Safety
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Teva Recalls Amphetamine Tablets Due to Impurities
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ICH Recommends Limited Use of Pharmaceutical Solvent
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EMA Pilot Seeks to Improve Postmarket Safety Data
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ICH Updates Guidance on Two Pharmaceutical Solvents
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