Frestedt Joy, Magurany Kelly
Regulatory Affairs, Abbott Nutrition, 3300 Seltzer Road, Columbus OH 43219, United States.
Alimentix, 9445 Minnetonka Boulevard, Saint Louis Park, MN 55426, United States.
Food Chem Toxicol. 2017 Jul;105:140-150. doi: 10.1016/j.fct.2017.03.064. Epub 2017 Mar 31.
After publication of the draft Generally Regarded As Safe (GRAS) rule in 1997, the United States (US) Food and Drug Administration (FDA) initiated an Interim Pilot Program encouraging the notification to FDA of GRAS determinations. This paper analyzes GRAS notifications submitted during the Interim Pilot Program along with warning letters issued during the same time period to better understand the evolution of the program and anticipate the future GRAS landscape. The success of the GRAS Notification program is demonstrated by the increasing rate of GRAS Notifications submitted to the FDA during the Interim Pilot Program, as well as the shift from a primarily domestic process to a process featuring an equal to greater contribution of GRAS Notifications from companies outside the US. Analysis of the first 600 GRAS Notifications revealed a number of interesting trends regarding the inclusion and composition of GRAS Expert Panels; differences in notifications for substances with nutritive, processing aid, or effect; and the duration of GRAS Notifications. The review of FDA warning letters associated with GRAS issues provides additional insight into GRAS notices, from the perspective of ongoing post-market emphasis on food safety with the implementation of the GRAS Final Rule.
1997年《一般认为安全(GRAS)》规则草案发布后,美国食品药品监督管理局(FDA)启动了一项临时试点计划,鼓励向FDA通报GRAS认定情况。本文分析了临时试点计划期间提交的GRAS通报以及同一时期发出的警告信,以便更好地了解该计划的演变情况,并预测GRAS的未来发展态势。临时试点计划期间提交给FDA的GRAS通报数量不断增加,以及从主要由国内企业参与的流程转变为美国以外公司提交的GRAS通报贡献相当甚至更大的流程,都证明了GRAS通报计划的成功。对前600份GRAS通报的分析揭示了一些关于GRAS专家小组的组成和成员情况、营养物质、加工助剂或功效物质通报的差异以及GRAS通报持续时间的有趣趋势。从随着GRAS最终规则的实施而持续进行的上市后食品安全重点工作的角度来看,对与GRAS问题相关的FDA警告信的审查为GRAS通报提供了更多见解。