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Food and Drug Administration Regulations Requiring Manufacturers To Assess the Safety and Effectiveness of New Drugs and Biological Products in Pediatric Patients
ProQuest Congressional Research Digital Collection: Part C (2011 forward) Available online
View online- Format:
- Book
- Government document
- Author/Creator:
- United States. General Accounting Office, issuing body.
- Language:
- English
- Subjects (All):
- United States. Food and Drug Administration.
- United States.
- Biological products--Law and legislation.
- Biological products.
- Drugs--Law and legislation.
- Drugs.
- Pediatrics.
- Physical Description:
- 1 online resource
- Contained In:
- ProQuest U.S. Congressional Research Digital Collection
- Place of Publication:
- Bethesda, Md. ProQuest 1998
- Notes:
- "Dec. 21, 1998"
- Record is based on bibliographic data in ProQuest U.S. Congressional Research Digital Collection. Reuse of record except for individual research requires license from ProQuest, LLC
- Vendor supplied data
- Publisher Number:
- cmp20222775
- crdccmp1998gao2210951
- CMP-1998-GAO-2210951
- Access Restriction:
- Restricted for use by site license
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