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OIG: FDA Increasing Generic Preapproval Inspections
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Two More Compounders Warned for Poor Sterile Manufacturing
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FDA to Fund Research on Further Use of Quality Metrics
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Woodcock: FDA Wants Mutual Inspection Program With Europe
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Industry Seeks Clarification on New EU GMP Mandates
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EMA Clarifies Reporting Requirements for Nonserious Medication Errors
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FDA Seizes Over $15 Million in Unapproved Topical Drugs
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Petition Asks FDA to Clarify Particulate Requirements in Injectable Drugs
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New Zealand Clarifies Pharmacovigilance Requirements for Drugmakers
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Counterfeit Botox Turns Up in the U.S., FDA Warns
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FDA Evaluating Regulations for Homeopathic Drugs
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PIC/S Adopts Same Risk Management GMPs as EU
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