 ... a drug and the methods used in, or the facilities or controls used for, its manufacture, processing, packing or holding do not conform to or are not operated or administered in conformity with current good manufacturing practice to assure that such...  Competitive Problems in the Drug Industry - 8341. lappuseautors: United States. Congress. Senate. Select Committee on Small Business. Subcommittee on Monopoly - 1971Pilnskats - Par šo grāmatu
 | United States - 1964 - 1098 lapas
...current good manufacturing practice to assure that such drug meets the requirements of this chapter as to safety and has the identity and strength, and...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... | |
 | United States - 1977 - 1276 lapas
...current good manufactuing practice to assure that such drug meets the requirements of this chapter as to safety and has the identity and strength, and...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... | |
 | 1969 - 668 lapas
...§5133.3-133.13, inclusive, shall apply in determining whether the methods used in, or the facilities or controle used for, the manufacture, processing, packing, or...as required by section 501 (a) (2) (B) of the act. The regulations in this Part 133 permit the use of precision automatic mechanical or electronic equipment... | |
 | 1971 - 676 lapas
...administered in conformity with current good manufacturing practice to assure that a medicated feed meets the requirements of the act as to safety, and...as required by section 501 (a) (2) (B) of the act. The regulations in this Part 133 permit the use of precision, automatic, mechanical, or electronic... | |
 | 2000 - 264 lapas
...in conformity with current good manufacturing practice to assure that a Type A medicated article(s) meets the requirements of the act as to safety, and...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 precision, automatic, mechanical,... | |
 | 1992 - 208 lapas
...in conformity with current good manufacturing practice to assure that a Type A medicated article(s) meets the requirements of the act as to safety, and...is represented to possess, as required by section 501(a) (2KB) of the act. The regulations in this part 226 permit the use of precision, automatic, mechanical,... | |
 | 1974 - 402 lapas
...operated or administered In conformity with, current good manufacturing practice to assure that any such drug meets the requirements of the act as to safety...characteristics, which it purports or is represented to possess, unless the manufacture, processing, packing, and holding of such drugs conform to the licensing and... | |
 | 1997 - 200 lapas
...conformity with current good manufacturing prac-tice to assure that such drug meets the requirement of the act as to safety and has the Identity and strength,...characteristics, which it purports or is represented to possess. (b)(l) The provisions of this part set forth the criteria for determining whether the manufacture of... | |
 | 1993 - 192 lapas
...conformity with current good manufacturing practice to assure that such drug meets the requirement of the act as to safety and has the identity and strength,...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... | |
 | 2000 - 232 lapas
...that a Type A medicated article(s) meets the requirements of the act as to §226.10 safety, and lias the identity and strength, and meets the quality and...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 precision, automatic, mechanical,... | |
| |
