Fed Regist. 2001 Nov 27;66(228):59138-61.
The Food and Drug Administration (FDA) is issuing a final rule to amend its regulations pertaining to the registration of foreign establishments and the listing of human drugs, animal drugs, biological products, and devices. The final rule requires foreign establishments whose products are imported or offered for import into the United States to register with FDA and to identify a United States agent. The final rule implements section 417 of the Food and Drug Administration Modernization Act of 1997 (FDAMA) as it pertains to foreign establishment registration.
美国食品药品监督管理局(FDA)正在发布一项最终规则,以修订其关于外国机构注册以及人用药品、动物药品、生物制品和器械清单的法规。该最终规则要求其产品进口或拟进口到美国的外国机构向FDA注册并指定一名美国代理人。该最终规则实施了1997年《食品药品管理局现代化法案》(FDAMA)中与外国机构注册相关的第417条。