2 options
U.S. Drug Approval Process : A Primer.
- Format:
- Book
- Government document
- Author/Creator:
- Library of Congress. Congressional Research Service.
- Language:
- English
- Subjects (All):
- Medical laws and legislation.
- Medicine--Research.
- Medicine.
- Product safety.
- Physical Description:
- 1 online resource (19 pages) : digital, PDF file
- monochrome
- Place of Publication:
- [Place of publication not identified] : [publisher not identified], 2001.
- System Details:
- System requirements: PDF reader software.
- text file
- Summary:
- Gives historical background and examines the FDA drug approval process and post-marketing surveillance. Reviews how "drug" is defined under Federal law, examines drug safety and effectiveness, preclinical research and testing, the drug application process, clinical trials, FDA review, and generic drug approval.
- Notes:
- CRS Report.
- Record is based on bibliographic data in ProQuest U.S. Congressional Research Digital Collection (last viewed July 2010). Reuse except for individual research requires license from ProQuest, LLC.
- Other Format:
- Microfiche version: Library of Congress. Congressional Research Service. U.S. Drug Approval Process
- Access Restriction:
- Restricted for use by site license.
The Penn Libraries is committed to describing library materials using current, accurate, and responsible language. If you discover outdated or inaccurate language, please fill out this feedback form to report it and suggest alternative language.