《医疗器械生产监督管理办法》

《医疗器械生产监督管理办法》       【英】

the Provisions for the Supervision and Management of Medical Device Production

Assessment Report on the Implementation of the National Human Rights Action Plan of China (2012-2015)

《国家人权行动计划（2012-2015年）》实施评估报告

1. 国务院修改《医疗器械监督管理条例》，国家食品药品监督管理总局审核发布《医疗器械生产监督管理办法》《医疗器械经营监督管理办法》《药品经营质量管理规范》《药品医疗器械飞行检查管理办法》等一系列规章。

1. The State Council also revised the Regulations for the Supervision and Administration of Medical Devices. The China Food and Drug Administration has reviewed and issued a series of regulations including the Provisions for the Supervision and Management of Medical Device Production, the Provisions for the Supervision and Management of Medical Device Operation, the Regulations on the Quality of Operation of Pharmaceutical Products and the Provisions for the Flight Check of Pharmaceutical Products and Medical Devices.