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" ... a full list of the articles used as components of such drug; (3) a full statement of the composition of such drug; (4) a full description of the methods used in, and the facilities and controls used for, the manufacture, processing, and packing of... "
False and Misleading Advertising: (prescription Tranquilizing Drugs) - 142. lappuse
autors: United States. Congress. House. Committee on Government Operations - 1958 - 268 lapas
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Decisions of the Commissioner of Patents and of the United States Courts in ...

United States. Patent Office - 1964 - 972 lapas
...articles used as components of such drug; (e) a full statement of the composition of such drug; (d) a fall description of the methods used in, and the facilities...manufacture, processing, and packing of such drug; (3) such samples of such drug and of the articles used as components thereof as tne * may require;...
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United States Congressional Serial Set, 10293. izdevums

1939 - 1496 lapas
...the articles used as components of such drug; (3) a full statement of the composition of such drug; (4) a full description of the methods used in, and...processing, and packing of such drug; (5) such samples of such drug and of the articles used as components thereof as the Secretary may require; and (6) specimens...
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The Code of Federal Regulations of the United States of America ..., 3. grāmata

1939 - 1554 lapas
...articles used as components of such drug; (d) A full statement of the composition of such drug; (e) A full description of the methods used in, and the...manufacture, processing, and packing of such drug; (f ) A full description of, or references to publications containing practical and accurate tests and...
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United States Code, 2. sējums

United States - 1964 - 1098 lapas
...the articles used as components of such drug; (3) a full statement of the composition of such drug; (4) a full description of the methods used in. and...processing, and packing of such drug; (5) such samples of such drug and of the articles used as components thereof as the Secretary may require; and (6) specimens...
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United States Code, 6. sējums

United States - 1977 - 1276 lapas
...relies as a basis for approval of his application with respect to the use of such drug in such feed, (C) a full description of the methods used in, and the...for, the manufacture, processing, and packing of such animal feed, (D) specimens of the labeling proposed to be used for such animal feed, and (E) if so...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1956 - 1164 lapas
...articles used as components of such drug; (d) A full statement of the composition of such drug; (e) A full description of the methods used in, and the...manufacture, processing, and packing of such drug; (f ) A full description of, or references to publications containing practical and accurate tests and...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1981 - 1252 lapas
...for any additional data or changes in the application to facilitate its consideration. (b) When the description of the methods used in, and the facilities...manufacture, processing, and packing of such drug appears adequate on its face, but it is not feasible to reach a conclusion as to the safety and effectiveness...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1977 - 1080 lapas
...for any additional data or changes in the application to facilitate its consideration. (b) When the description of the methods used in, and the facilities...manufacture, processing, and packing of such drug appears adequate on its face, but it is not feasible to reach a conclusion as to the safety and effectiveness...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1980 - 718 lapas
...applicant will be furnished written comment on any apparent deficiencies in the application. (b) When the description of the methods used in, and the facilities...for, the manufacture, processing, and packing of such new animal drug appears adequate on its face, but it is not feasible to reach a conclusion as to the...
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The Code of Federal Regulations of the United States of America

1964 - 1242 lapas
...declaration should be designated as such and percent excess shown. Reasonable variations may be specified. 4. A full description of the methods used In, and the facilities and controls used for, the manufacture, processing, and packing of the drug. Included in this description...
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