Fed Regist. 2005 Nov 23;70(225):70720-30.
The Food and Drug Administration (FDA) is amending its regulations on the exportation of investigational new drugs, including biological products. The final rule describes four different mechanisms for exporting an investigational new drug product. These provisions implement changes in FDA's export authority resulting from the FDA Export Reform and Enhancement Act of 1996 and also simplify the existing requirements for exports of investigational new drugs.
美国食品药品监督管理局(FDA)正在修订其关于包括生物制品在内的研究性新药出口的法规。最终规则描述了出口研究性新药产品的四种不同机制。这些规定实施了1996年《FDA出口改革与增强法案》带来的FDA出口权限变化,同时也简化了研究性新药出口的现有要求。