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Food and Drug Administration |
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Current Good Manufacturing Practices |
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Health, Education, and Welfare (1953) |
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Prescription Drug User Free Act (1992) |
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Best Pharmaceuticals for Children Act (2002) |
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Medical Device User Free and Modernization Act (2002) |
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Biologics Price Competition Innovation Act (2009) |
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Consumer Product Safety Commision |
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Drug Enforcement Administration |
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Environmental Protection Agency |
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U.S. Department of Agriculture |
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Office of Minority Health |
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Center for Drug Evaluation and Research |
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Center for Biologics Evaluation and Research |
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Center for Devices and Radiological Health |
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Center for Tobacco Products |
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Office of Regulatory Affairs |
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Office of International Programs |
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Center for Veterinary Medicine |
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Center for Food Safety and Applied Nutrition |
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National Center for Toxicological Research |
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Office of Counter-terrorism and Emerging Threats |
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Office of Regulatory Science and Innovation |
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Notional Archives and Records Administration |
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Code of Federal Regulations |
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Safety, Identity, Strength, Quality, and Purity or (ISQP): drop safety |
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Active Pharmaceutical Ingredient |
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American Society for Testing and Materials |
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Failure Mode Effects Analysis (FMECA): criticality |
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Hazard Analysis and Critical Control Points |
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Hazard Operability Analysis |
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Preliminary Hazard Analysis |
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International Code on Harmonization |
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International Society for Pharmaceutical Engineering |
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