医学信息Issue(14)：333-334,2.
规范国产药包材再注册申报资料要求
Specification the Re-registration of Domestic Drug Packaging Materials Requirements
王姝 1张颖 1李松波 1富晓楠 1梁健2
作者信息
- 1. 辽宁省食品药品监督管理局行政服务中心，辽宁 沈阳 110003
- 2. 江西中医药大学，江西 南昌 330004
- 折叠
摘要
Abstract
In 2014 April national institutes for food and drug control issued on the "application for technical evaluation of packaging production data reporting requirements" and other six reporting requirements of the notice.Based on the analysis of management situation in China on the drug packaging materials,Combined with the actual situation of the medicine packing material production to the application for the registration of the common problems in the acceptance review summary analysis,the author puts forward some thinking and measures to improve and to strengthen the domestic drug packaging materials re registration management,in order to provide some ef ective reference for drug packaging materials production enterprises and supervision department.关键词
药包材再注册/申报资料要求/监管Key words
Re-registration of drug packaging materials/Registration requirements/Supervision引用本文复制引用
王姝,张颖,李松波,富晓楠,梁健..规范国产药包材再注册申报资料要求[J].医学信息,2015,(14):333-334,2.
