Fed Regist. 1998 May 14;63(93):26744-55.
The Food and Drug Administration (FDA) is proposing to require manufacturers of certain human cellular and tissue-based products to register with the agency and list their products. In addition, the agency is proposing to amend the registration and listing regulations that currently apply to human cellular and tissue-based products regulated as drugs, devices, and/or biological products. This action is being taken to establish a unified registration and listing program for human cellular and tissue-based products.
美国食品药品监督管理局(FDA)提议要求某些人体细胞和组织制品的制造商向该机构进行注册并列出其产品。此外,该机构还提议修订目前适用于作为药品、器械和/或生物制品进行监管的人体细胞和组织制品的注册和列表规定。采取这一行动是为了建立一个针对人体细胞和组织制品的统一注册和列表计划。