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" ... products conform to appropriate standards of identity, strength, quality, and purity. Laboratory controls shall include... "
Drug Safety: Hearings Before a Subcommittee of the Committee on Government ... - Page 1443
by United States. Congress. House. Committee on Government Operations - 1964 - 2377 pages
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The Code of Federal Regulations of the United States of America

Administrative law - 1969 - 668 pages
...include the establishment of adequate specifications and test procedures to assure that components, drug preparations in the course of processing, and...samples. Such records shall also provide for appropriate retesting of materials subject to deterioration. (b) The establishment of appropriate specifications,...
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Code of Federal Regulations: Containing a Codification of Documents of ...

Administrative law - 1974 - 402 pages
...adequate specifications and test procedures to assure that the drug components and the medicated premixes conform to appropriate standards of identity, strength,...master records containing appropriate specifications and a description of the test proChapter I — Food and Drug Administration cedures used to check them...
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The Code of Federal Regulations of the United States of America

Administrative law - 1993 - 192 pages
...the drug components and the Type A medicated article(s) conform to appropriate standards of fdentity, strength, quality, and purity. Laboratory controls...master records containing appropriate specifications and a description of the test procedures used to check them for each kind of drug component used in...
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Code of Federal Regulations: Containing a Codification of Documents of ...

Administrative law - 1997 - 200 pages
...assure that components, drug product containers, closures, in-process materials, labeling, and drug products conform to appro-priate standards of identity,...quality, and purity. Laboratory con-trols shall include: (1) Determination of conformance to appropriate written specifications for the acceptance of each lot...
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The Code of Federal Regulations of the United States of America

Administrative law - 2003 - 210 pages
...assure that components, drug product containers, closures, in-process materials, labeling, and drug products conform to appropriate standards of identity,...quality, and purity. Laboratory controls shall include: (1) Determination of conformance to appropriate written specifications for the acceptance of each lot...
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Code of Federal Regulations: Containing a Codification of Documents of ...

Administrative law - 1992 - 208 pages
...assure that components, drug product containers, closures, in-process materials, labeling, and drug products conform to appropriate standards of identity,...quality, and purity. Laboratory controls shall include: ( 1 ) Determination of conf ormance to appropriate written specifications for the acceptance of each...
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Competitive Problems in the Drug Industry, Volume 21

United States. Congress. Senate. Select Committee on Small Business. Subcommittee on Monopoly - Pharmaceutical industry - 1971 - 304 pages
...appropriate specifications, standards, and test procedures to assure that components, in-processed drugs, and finished products conform to appropriate standards...records containing appropriate specifications for the acceptance of each lot of drug components, product containers, and their components, used in drug...
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Competitive problems in the drug industry: hearings before Subcommittee on ...

United States. Congress. Senate. Select Committee on Small Business. Subcommittee on Monopoly - Pharmaceutical industry - 1967 - 410 pages
...specifications and test procedures to assure that the drug components and the finished medicated feeds conform to appropriate standards of identity, strength,...master records containing appropriate specifications and a description of the test procedures used to check them for each kind of drug used in the manufacture...
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Competitive Problems in the Drug Industry, Volume 24

United States. Congress. Senate. Select Committee on Small Business. Subcommittee on Monopoly - Pharmaceutical industry - 1967 - 866 pages
...laboratory controls that include adequate specifications and test procedures to insure that components, drug preparations in the course of processing, and...standards of identity, strength, quality, and purity. --Maintain, for at least 2 years, complete records of the distribution of each batch of drug in a manner...
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Hearings, Reports and Prints of the Senate Select Committee on ..., Parts 20-22

United States. Congress. Senate. Select Committee on Small Business - Legislative hearings - 1971 - 1192 pages
...appropriate specifications, standards, and test procedures to assure that components, in-processed drugs, and finished products conform to appropriate standards...records containing appropriate specifications for the acceptance of each lot of drug components, product containers, and their components, used in drug...
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