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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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Definition
| U.S. Department of Agriculture |
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| Office of Minority Health |
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Definition
| Center for Drug Evaluation and Research |
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| Center for Biologics Evaluation and Research |
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Definition
| 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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Definition
| Office of International Programs |
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Definition
| Center for Veterinary Medicine |
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Definition
| Center for Food Safety and Applied Nutrition |
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Definition
| National Center for Toxicological Research |
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| Office of Counter-terrorism and Emerging Threats |
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Definition
| Office of Regulatory Science and Innovation |
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Definition
| Notional Archives and Records Administration |
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Definition
| Code of Federal Regulations |
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Definition
| 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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Definition
| Hazard Analysis and Critical Control Points |
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Definition
| Hazard Operability Analysis |
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Definition
| Preliminary Hazard Analysis |
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| International Code on Harmonization |
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| International Society for Pharmaceutical Engineering |
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