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FDA's Authority to Regulate Drug Compounding : A Legal Analysis.
ProQuest Congressional Research Digital Collection: Part C (2011 forward) Available online
View online- Format:
- Book
- Government document
- Author/Creator:
- Library of Congress. Congressional Research Service. American Law Division.
- Language:
- English
- Subjects (All):
- Judge-made law.
- Drugs.
- Medical laws and legislation.
- Pharmaceutical industry.
- Physical Description:
- 1 online resource (1 online resource (14 p), digital, PDF file)
- monochrome
- Place of Publication:
- [Place of publication not identified] : [publisher not identified], 2010.
- System Details:
- text file
- Summary:
- Provides historical overview of FDA regulation of drug compounding, the process in which a pharmacist combines, mixes, or alters various drug ingredients to create a medication for an individual patient in response to a practitioner's prescription. Reviews decisions in Thompson v. Western States Medical Center and Medical Center Pharmacy v. Mukasey . Addresses 2002 FDA compliance policy guide and FDA authority to regulate drug compounding and possible future developments.
- Notes:
- Record is based on bibliographic data in ProQuest U.S. Congressional Research Digital Collection (last viewed Apr. 2014). Reuse except for individual research requires license from ProQuest, LLC.
- CRS Report.
- Other Format:
- Microfiche version: Library of Congress. Congressional Research Service. American Law Division. FDA's Authority to Regulate Drug Compounding
- Access Restriction:
- Restricted for use by site license.
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