Fed Regist. 1998 Sep 23;63(184):50815.
The Food and Drug Administration (FDA) is correcting a proposed rule that appeared in the Federal Register of June 16, 1998 (63 FR 32772). The document proposed to amend the FDA regulations governing the review of agency decisions by inserting a statement that sponsors, applicants, or manufacturers of drugs (including biologics) or devices may request review of a scientific controversy by an appropriate scientific advisory panel, or an advisory committee. The document was published with an error. This document corrects that error.
美国食品药品监督管理局(FDA)正在纠正一项出现在1998年6月16日《联邦公报》(63 FR 32772)上的拟议规则。该文件提议修订FDA关于审查机构决定的法规,插入一项声明,即药品(包括生物制品)或器械的申办者、申请人或制造商可请求由适当的科学咨询小组或咨询委员会对科学争议进行审查。该文件发布时存在错误。本文件纠正了该错误。