U. S. Food and Drug Administration. (2011) Advancing Regulatory Science at FDA: A Strategic Plan. Project Report. U. S. Food and Drug Administration.
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Abstract
The core responsibility of FDA is to protect consumers by applying the best possible science to its regulatory activities — from pre-market review of efficacy and safety to post-market product surveillance to review of product quality. FDA has developed a strategic plan for regulatory science, the science of developing new tools, standards, and approaches to assess the safety, efficacy, quality, and performance of FDA-regulated products.
Item Type: | Monograph (Project Report) |
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InterNano Taxonomy: | Social and Economic Impacts > Policy and Regulation |
Collections: | Nanomanufacturing Report Collection |
Depositing User: | Robert Stevens |
Date Deposited: | 31 Aug 2011 15:56 |
Last Modified: | 31 Aug 2011 15:56 |
URI: | http://eprints.internano.org/id/eprint/1691 |
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