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" ... conform to or are not operated or administered in conformity with current good manufacturing practice to assure that such drug meets the requirements of this Act as to safety and has the identity and strength, and meets the quality and purity characteristics,... "
Predator Control and Related Problems: Hearings Before Subcommittee on ... - Страница 41
по United States. Congress. Senate. Committee on Appropriations. Subcommittee on Agriculture, Environmental and Consumer Protection - 1971 - 220 страници
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United States Code, Том 6

United States - 1977 - 1276 страници
...drug meets the requirements of this chapter as to safety and has the identity and strength, and meets the quality and purity characteristics, which it purports or is represented to possess; or (3) if its container is composed, in whole or in part, of any poisonous or deleterious substance...

United States Code, Том 2

United States - 1964 - 1098 страници
...drug meets the requirements of this chapter as to safety and has the identity and strength, and meets the quality and purity characteristics, which it purports or is represented to possess; or (3) if it is a drug and its container is composed, in whole or in part, of any poisonous or deleterious...

Code of Federal Regulations: Containing a Codification of Documents of ...

1997 - 200 страници
...article(s) meets the requirements of the act as to safety, and has the identity and strength, and meets the quality and purity characteristics which it purports or is represented to possess, as required by section 501(a) (2)(B) of the act. The regulations in this part 226 permit the use of...

The Code of Federal Regulations of the United States of America

1993 - 192 страници
...such drug meets the requirement of the act as to safety and has the identity and strength, and meets the quality and purity characteristics, which it purports or is represented to possess. (b)(1) The provisions of this part set forth the criteria for determining whether the manufacture of...

Drug Industry Act of 1962: Hearings ... Eighty-seventh Congress, Second ...

United States. Congress. House. Committee on Interstate and Foreign Commerce - 1962 - 734 страници
...manufacturing practice to assure that such drug or animal feed has the identity and strength, and meets the quality and purity characteristics, which it purports or is represented to possess. Under these provisions, it would no longer be necessary to require the filing of new animal drug applications...

Drug Industry Act of 1962, Hearings ... 87-2 ... June 19, 20, 21, 22, August ...

United States. Congress. House. Interstate and Foreign Commerce - 1962 - 732 страници
...manufacturing practice to assure that such drug or animal feed has the identity and strength, and meets the quality and purity characteristics, which it purports or is represented to possess. Under these provisions, it would no longer be necessary to require the filing of new animal drug applications...

Compilation of Selected Public Health Laws ...

United States. Congress. House Interstate and Foreign Commerce - 1966 - 574 страници
...such drug meets the requirements of this Act as to safety and has the identity and strength, and meets the quality and purity characteristics, which it purports or is represented to possess; or (3) if it is a drug and its container is composed, in whole or in part, of any poisonous or deleterious...

Small Business Problems in the Drug Industry: Hearings Before the ..., Том 2

United States. Congress. House. Select Committee on Small Business. Subcommittee on Activities of Regulatory Agencies - 1967 - 978 страници
...such drug meets the requirements of the ACT as to safety and has the identity and strength, and meets the quality and purity characteristics, which it purports or is represented to possess. Part 133 of the regulations outlines the criteria for conformation to current good manufacturing practice....

Competitive Problems in the Drug Industry, Том 33

United States. Congress. Senate. Select Committee on Small Business. Subcommittee on Monopoly - 1967 - 1118 страници
...drugs would meet the requirements of the Federal Food, Drug, and Cosmetic Act as to safety and would have the Identity and strength and meet the quality and purity characteristics which they purported and were represented to possess; (all Counts) and 351(c) In that said drugs were not...

Competitive Problems in the Drug Industry, Том 24

United States. Congress. Senate. Select Committee on Small Business. Subcommittee on Monopoly - 1967 - 866 страници
...drug meets the requirements of the FDfjC Act as to safety, and has the identity and strength and meets the quality and purity characteristics which it purports or is represented to possess, as required by section 501(a)(2)(B) of the FD§C Act. A brief description of each GMP regulation follows-....




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