Publication
18 May 2012
This research report discusses the role of the Food and Drug Administration in regulating the safety and effectiveness of drugs sold in the US. It is done in two phases: the approval of new drugs heading to market, and the regulating of approved drugs including proper use and advertising.
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English (PDF, 23 pages, 376 KB) |
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Author | Susan Thaul |
Series | US Congressional Research Service Reports |
Publisher | US Government |