U. S. Food and Drug Administration. (2011) Advancing Regulatory Science at FDA: A Strategic Plan. Project Report. U. S. Food and Drug Administration.
FDA's_Regulatory_Science_Strategic_Plan_corrected_8-17-11.pdf - Published Version
Download (3718Kb) | Preview
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)|
|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|
Actions (login required)