Actions for Drug Safety and Effectiveness [electronic resource] : Issues and Action Options After FDA Approval

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Drug Safety and Effectiveness [electronic resource] : Issues and Action Options After FDA Approval

Corporate Author
Library of Congress. Congressional Research Service
Published
[Place of publication not identified] : [publisher not identified], 2007.
Physical Description
40 pages : digital, PDF file
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Summary
Examines issues related to drug safety in the context of the regulatory process that Congress and the FDA have established for ensuring that drugs are safe and effective. Describes FDA process for approving new drugs, and examines FDA and industry role in postmarket regulation of approved drugs. Discusses problems in identifying and resolving postmarketing safety and effectiveness issues, and outlines FDA and Congressional options for improving postmarket activities.
Subject(s)
Related Titles
ProQuest U.S. Congressional Research Digital Collection
Note
Record is based on bibliographic data in ProQuest U.S. Congressional Research Digital Collection (last viewed Dec. 2010). Reuse except for individual research requires license from ProQuest, LLC.
CRS Report.
AVAILABLE ONLINE TO AUTHORIZED PSU USERS.
Technical Details
System requirements: PDF reader software.
View MARC record | catkey: 10112384