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FDA Slaps Second Impax Plant with a Form 483
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EU Regulators Seek Information on Products Tested by GVK Bio
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Bribery Allegations Continue to Hound GlaxoSmithKline in China, Elsewhere
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FDA Warns Italian API Maker for Deleting Quality Data
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Compounding Pharmacy Relents to FDA’s Recall Request
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FDA Issues Safety Alert for Texas Compounder’s Products
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FDA Releases Slew of Warnings to Compounding Pharmacies
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Lack of Testing, Data Integrity Means 483 for OTC Drugmaker
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No Batch Records or Inspections Lands API Maker a Form 483
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Insects and Leaky Products Get Hospira Latest 483
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FDA: Five-Year Strategic Plan to Boost International Partnerships
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FDA Plans to Increase Scrutiny of Drugmakers with Poor Data Integrity
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