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FDA Quality Metrics Program Delayed, Extended to Biologic Products
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Drugmakers Win Four-Month Reprieve from Product Tracing Requirement
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FDA Warns Italian API Maker for Deleting Quality Data
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Actavis Recalls Liquid Antibiotic in New Zealand
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Baxter Recalls IV Solutions Due to Presence of Particles
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Sun Pharma Recalls Generic Over Stability Issues
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Compounding Pharmacy Relents to FDA’s Recall Request
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Persistent Particulates Cause Latest Hospira Recall
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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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