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Definition
| Clinical Laboratories Improvement Amendments of 1988 |
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Definition
| Chemistry and Manufacturing Controls |
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Definition
| Contract Management Organization |
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Definition
| Centers for Medicare and Medicaid Services Admin for SCHIP, HIPAA, & CLIA. |
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Definition
| Code of Ethics or Certificate of Exportability |
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Definition
| Consumer Products Safety Commission |
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Definition
| Clinical Research Coordinator |
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Definition
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Definition
| Contract Research Organization |
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Definition
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Definition
| Consumer Safety Officer - usually contract person at FDA. Also known as Project Manager |
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Definition
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Term
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Definition
| Clinical Trial Certificate |
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Term
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Definition
| Common Technical Document |
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Definition
| Center for Veterinary Medicine |
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Definition
| Division of Drug Marketing, Advertising and Commmunications (CDER) |
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Definition
| Drug Enforcement Administration |
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Term
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Definition
| Design History File- Describes design of a finished device |
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Term
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Definition
| Design History Record - Contains the production history of a device |
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Definition
| Drug Master File - Submission to FDA that may be used to provide confidential detailed information about facilities, processes or articles used in the processing, packaging, and storing one or more human drugs. |
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Definition
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Term
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Definition
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Definition
| Drug Quality Reporting System |
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Definition
| Data and Safety Monitoring Board |
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Definition
| Division of Small Manufacturers, International and Consumer Assistance (CDRH) |
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Definition
| Direct-to-Consumer (advertising) |
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Definition
| Environmental Impact Assessment |
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Definition
| Establishment Inspection Report |
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Definition
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Definition
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Definition
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Term
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Definition
| Food, Drug and Cosmetics Act of 1938 |
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Definition
| Food and Drug Administration |
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Definition
| Food and Drug Administration Modernization Act of 1997 |
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Definition
| Freedom of Information Act of 1966 |
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Definition
| Fair Packaging and Labeling Act |
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Definition
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Term
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Definition
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Term
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Definition
| Fiscal Year (FDA = Oct. - Sept) |
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Definition
| General Agreement of Tariffs and Trade |
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Definition
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Definition
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Definition
| Global Harmonization Task Force |
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Term
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Definition
| Good Laboratory Practices |
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Definition
| Good Manufacturing Practices |
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Term
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Definition
| Generally Recognized as Safe (and Effective) |
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