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Definition
| Competent Authority (regulatory body charged with monitoring compliance with European Union member state national statutes and regulations |
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Definition
| Cancer Biomedical Informatics Grid |
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| Cancer Data Standards Repository and toolset maintained by NCI |
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Definition
| Canadian Association of Professional Pharmaceutical Regulatory Affairs (also ACPR) |
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Definition
| Chemical Abstracts Service |
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Definition
| Center for Biologics Evaluation and Research (FDA) |
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Definition
| Committee on Clinical Investigations |
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Definition
| Comite Consultative pur la Protection des Personnes dans les Recherches Biomedicales (France) |
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Definition
| Certified Clinical Research Associate |
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Definition
| Certified Clinical Research Coordinator |
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Definition
| Certified Clinical Research Professional |
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Definition
| Company Core Safety Information |
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Definition
| Clinical Document Architecture |
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| Clinical Data Acquisition Standards Harmonization |
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Definition
| Centers for Disease Control and Prevention |
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| Center for Drug Evaluation and Research (FDA) |
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| Clinical Data Interchange Standards Consortium |
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Definition
| clinical data management system |
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Definition
| Center for Devices and Radiological Health (FDA) |
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Definition
| Comite Europeen de Normalisation (European Committee for Standardization) |
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Definition
| Continuing Education Unit |
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Definition
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Term
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Definition
| Code of Federal Regulations |
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Term
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Definition
| current good manufacturing practices |
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Definition
| Consolidated Health Informatics |
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Definition
| Committee on Human Research |
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Definition
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Definition
| Council for International Organisations of Medical Sciences (postapproval international ADR reporting, UK) |
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Term
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Definition
| Certified IRP professional |
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Definition
| Commonwealth of Independent States |
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Definition
| Clinical Laboratory Improvement Amendments |
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Definition
| concentration maximum; used in PK & BE to indicate maximum plasma concentration for a drug |
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Term
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Definition
| chemistry, manufacturing, and control |
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Term
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Definition
| Continuing Medical Education |
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Definition
| Centers for Medicare and Medicaid Services |
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Definition
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Term
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Definition
| Consolidated Standards of Reporting Trials |
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Term
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Definition
| CDISC Operating Process/Procedure |
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Term
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Definition
| CDISC Operational Roadmap Environment |
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Term
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Definition
| Coding Symbols for a Thesaurus of Adverse Reaction Terms |
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Definition
| Committee for the Protection of Human Subjects |
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Definition
| Committee for Proprietary Medicinal Products (EU) |
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Definition
| Consumer Product Safety Commission (US) |
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Definition
| clinical research associate |
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Definition
| Cooperative Research and Development Agreement (with US government entities) |
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Definition
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Definition
| clinical research coordinato |
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Definition
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Term
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Definition
| Central Research Information Exchange |
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Term
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Definition
| contract research organization |
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Definition
| Center for the Study of Drug Development |
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Definition
| Collaborative Standards Forum (CDISC) |
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Term
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Definition
| colony stimulating factor |
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Definition
| Committee on Safety of Medicines (UK) |
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| Computerized Systems Used in Clinical Investigations |
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| Clinical Trial Certificate (UK) |
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Definition
| Common Terminology Criterion for Adverse Events |
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Definition
| Common Technical Document |
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Definition
| Cancer Therapy Evaluation Program |
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Term
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Definition
| clinical trials materials |
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Definition
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Term
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Definition
| common unique identifier- a code used in the Enterprise Vocabulary System to link a particular concept across one or more terms |
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| Center for Veterinary Medicine (FDA) |
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| Drug Abuse Warning Network |
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Definition
| Department of Drugs (Sweden) |
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| Drug Enforcement Administration (US) |
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| Drug Efficacy Study Implementation notice (FDA, to evaluate drugs in use before 1962) |
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| German Society of Pharmaceutical Medicine |
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| Department of Health and Human Services |
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| Drug Information Association |
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| Digital Imaging and Communications in Medicine |
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Definition
| Data Management Biomedical (France) |
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Definition
| Drug Price Competition and Patent Term Restoration Act of 1984 |
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Definition
| Division of Scientific Investigations (FDA) |
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Definition
| data safety monitoring board |
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Definition
| Development of Standardized Nomenclature Project (FDA) |
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Definition
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Definition
| Draft Standard for Trial Use |
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| Development Safety Update Report (ICH) |
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| direct-to-consumer (drug advertising) |
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