 (1) the term 'manufacture, preparation, propagation, compounding, or processing' shall include repackaging or otherwise changing the container, wrapper, or labeling of any drug package in furtherance of the distribution of the drug from the original place...  Code of Federal Regulations 21 Parts 800 to 1299 Food and Drugs: Revised as ...autors: Office of the Federal Register, Office of the Federal Register (U.S.) Staff - 2006 - 796 lapasFragmentu skats - Par šo grāmatu
 | United States - 1975 - 1016 lapas
...container, wrapper, or labeling of any drug package in furtherance of the distribution of the drug from the original place of manufacture to the person...makes final delivery or sale to the ultimate consumer ; and (2) the term "name" shall include in the case of a partnership the name of each partner and,... | |
 | United States - 1977 - 436 lapas
...or labeling of any drug package or device package in furtherance of the distribution of the drug or device from the original place of manufacture to the...makes final delivery or sale to the ultimate consumer or user ; and (2) the term "name" shall include in the case of a partnership the name of each partner... | |
 | 1979 - 840 lapas
...container, wrapper, or labeling of any drug package in furtherance of the distribution of the drug from the original place of manufacture to the person...makes final delivery or sale to the ultimate consumer. (g) The definitions and interpretations contained in section 201 and 510 of the Federal Food, Drug,... | |
 | 1979 - 968 lapas
...container, wrapper, or labeling of any drug package in furtherance of the distribution of the drug from tbe original place of manufacture to the person who makes final delivery or sale to tbe ultimate consumer; "'(2) the term "name" shall Include In the case of a partnership the name of... | |
 | 1980 - 332 lapas
...•eciuired to have an approved premarc.et approval application as provided in « -<-l ion 515 of the act. CO "Establishment" means a place of Business under one...delivery or sale to the ultimate consumer; (2) Initial distribution of imported devices; or (3) Initiation of specifications for devices that are manufactured... | |
 | United States. Congress. House. Select Committee on Narcotics Abuse and Control - 1982 - 222 lapas
...container, wrapper, or labeling of any drug package . . .in furtherance of the distribution of the drug . . .from the original place of manufacture to the person...makes final delivery or sale to the ultimate consumer or user. . . ." 21 USC 360. The method chosen by Congress to ensure that FDA has such information is... | |
 | 1984 - 458 lapas
...required to have an approved premarket approval application as provided in section 515 of the act. (c) "Establishment" means a place of business under...place of manufacture to the person who makes final deliver;' r sale to the ultimate consumer; (2) Initial distribution of imported devices; or (3) Initiation... | |
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