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EMA Outlines Requirements for Manufacturing Finished Dosage Forms
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New Excipient GMPs in EU Take Effect in March
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Seven More Compounders in Trouble Over Sterility Issues
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FDA Requires Six-Month Notice for Potential Manufacturing Stoppages
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Indian Manufacturers See More Compliance Woes
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Hospira, Teva, Mylan and Baxter Recalls Pile Up
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EMA to Update Guideline on Risk Management Plans
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Disconnect Between Management, QCU Possible Source of Warning Letters
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European Drugmakers Move Closer to Implementing Counterfeit Repository
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Particulates Once More Behind Mylan Recall
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FDA and EMA Provide Details on Convergence
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OPQ Plans Team-Based Assessments As Part of Drug Review Process
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