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Drug regulation reform--oversight : New drug approval process : Hearing before the Subcommittee on Health and the Environment of the Committee on Interstate and Foreign Commerce, House of Representatives, Ninety-sixth Congress, second session.

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Bibliographic Details
Online Access: Search for the full-text version of this title in HathiTrust
Corporate Author: United States. Congress. House. Committee on Interstate and Foreign Commerce. Subcommittee on Health and the Environment
Other title:New drug approval process.
Orphan drugs.
Format: Government Document Book
Language:English
Published: Washington : U.S. G.P.O., 1980-
Subjects:
United States. > Food and Drug Administration.
Pharmaceutical policy > United States.
Drugs > United States > Testing.
Pharmaceutical industry > United States.
Drug Industry.
Pharmaceutical Preparations > standards.
Research > standards.
Drugs > Testing.
Pharmaceutical industry.
Pharmaceutical policy.
Description
Item Description:Volume 1: "Food and Drug Administration regulation of research, development, and marketing of drugs, June 25, 1980."
Volume 2: "How can we best use our limited resources and at the same time insure safe and effective drugs to diseases which occur infrequently, June 26, 1980."
"Serial number 96-170. Volume 1."
"Serial number 96-216."
Physical Description:2 volumes ; 23 cm.

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