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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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Canadian API Maker Warned for cGMP Failures, Will Remain on Import Alert
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Compounders Seeking Intervention to Stop Proposed MOU
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FDA Steps Up Global Enforcement Actions
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Cobweb Trips up South Carolina Drugmaker
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FDA and EMA Provide Details on Convergence
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FDA Clears Hospira to Produce Injectables at New India Plant
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Data Integrity Issues Fuel Rise In Critical Inspection Findings
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Guidance Targets Overfilling of Vials, Ampules
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FDA Tightens Screws on Compounders
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OPQ Plans Team-Based Assessments As Part of Drug Review Process
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