Advancing Regulatory Science at FDA: A Strategic Plan

U. S. Food and Drug Administration. (2011) Advancing Regulatory Science at FDA: A Strategic Plan. Project Report. U. S. Food and Drug Administration.

[img]
Preview
PDF
FDA's_Regulatory_Science_Strategic_Plan_corrected_8-17-11.pdf - Published Version

Download (3718Kb) | Preview

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)
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

Actions (login required)

View Item View Item