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A risk-characterization framework for decision-making at the Food and Drug Administration /
With the responsibility to ensure the safety of food, drugs, and other products, the U.S. Food and Drug Administration (FDA) faces decisions that may have public-health consequences every day. Often the decisions must be made quickly and on the basis of incomplete information. FDA recognized that co...
| Clasificación: | Libro Electrónico |
|---|---|
| Autor Corporativo: | |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
Washington D.C. :
National Academies Press,
[2011]
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| Colección: | Online access: National Academy of Sciences National Academies Press.
Online access: NCBI NCBI Bookshelf. |
| Temas: | |
| Acceso en línea: | Texto completo |
MARC
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| 110 | 2 | |a National Academies (U.S.). |b Committee on Ranking FDA Product Categories Based on Health Consequences, Phase II, |e author. | |
| 245 | 1 | 2 | |a A risk-characterization framework for decision-making at the Food and Drug Administration / |c Committee on Ranking FDA Product Categories Based on Health Consequences, Phase II, Board on Environmental Studies and Toxicolgoy, Division on Earth and Life Studies, National Research Council, Institute of Medicine, National Research Council of the National Academies. |
| 264 | 1 | |a Washington D.C. : |b National Academies Press, |c [2011] | |
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| 520 | 3 | |a With the responsibility to ensure the safety of food, drugs, and other products, the U.S. Food and Drug Administration (FDA) faces decisions that may have public-health consequences every day. Often the decisions must be made quickly and on the basis of incomplete information. FDA recognized that collecting and evaluating information on the risks posed by the regulated products in a systematic manner would aid in its decision-making process. Consequently, FDA and the Department of Health and Human Services (DHHS) asked the National Research Council (NRC) to develop a conceptual model that could evaluate products or product categories that FDA regulates and provide information on the potential health consequences associated with them. A Risk-Characterization Framework for Decision-Making at the Food and Drug Administration describes the proposed risk-characterization framework that can be used to evaluate, compare, and communicate the public-health consequences of decisions concerning a wide variety of products. The framework presented in this report is intended to complement other risk-based approaches that are in use and under development at FDA, not replace them. It provides a common language for describing potential public-health consequences of decisions, is designed to have wide applicability among all FDA centers, and draws extensively on the well-vetted risk literature to define the relevant health dimensions for decision-making at the FDA. The report illustrates the use of that framework with several case studies, and provides conclusions and recommendations. | |
| 536 | |a This project was supported by Contract HHSP23320042509XI/HHSP233200800001T between the National Academy of Sciences and the U.S. Department of Health and Human Services. Any opinions, findings, conclusions, or recommendations expressed in this publication are those of the authors and do not necessarily reflect the view of the organizations or agencies that provided support for this project. | ||
| 588 | 0 | |a Version viewed October 3, 2014. | |
| 505 | 0 | 0 | |t Introduction -- |t A Risk-Characterization Framework -- |t Case Study of a Mitigation-Selection Decision -- |t Case Study of a Targeting Decision -- |t Case Study of a Strategic-Investment Decision -- |t Case Study of a Targeting Decision That Spans Food and Drug Administration Centers -- |t Conclusions and Future Directions -- |g A: |t Letter Report on the Development of a Model for Ranking FDA Product Categories on the Basis of Health Risks -- |g B: |t Statement of Task for the Committee on Ranking FDA Product Categories Based on Health Consequences, Phase II -- |g C: |t Scenarios Provided by the U.S. Food and Drug Administration to the Committee on Ranking FDA Product Categories Based on Health Consequences, Phase II -- |g D: |t Biographic Information on the Committee on Ranking FDA Product Categories Based on Health Consequences, Phase II -- |g E: |t Factors Hypothesized as Important in Understanding Risk. |
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| 650 | 2 | 2 | |a Drug Approval |
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| 650 | 2 | 2 | |a United States Government Agencies |
| 650 | 6 | |a Prise de décision |z États-Unis |v Études de cas. | |
| 650 | 6 | |a Produits commerciaux |x Sécurité |z États-Unis |x Prise de décision |v Études de cas. | |
| 650 | 6 | |a Évaluation du risque |z États-Unis |v Études de cas. | |
| 650 | 6 | |a Prise de décision. | |
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