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第六届全国人大常委会第七次会议审议通过的《中华人民共和国药品管理法》将于一九八五年七月一日起施行。为了切实贯彻执行,加强医药行业的质量管理,确保人民用药安全、有效,特作以下规定: 一、省、自治区、直辖市及计划单列市医药管理局(总公司),要按照《药品管理法》规定的药品生产企业和药品经营企业必须具备的条件,抓紧对本地区的药品生产、
The “People’s Republic of China Drug Administration Law” reviewed and passed by the sixth session of the Standing Committee of the National People’s Congress will be implemented on July 1, 1985. In order to effectively implement the implementation, strengthen the quality management of the pharmaceutical industry and ensure the safety and effectiveness of people’s drug use, the following provisions are specially made: 1. The provincial, autonomous region, municipality directly under the Central Government and the City of Planned Medicines (Head Office) must comply with the Drug Administration Law. The conditions that must be met by the prescribed drug manufacturers and drug-manufactured enterprises, and pay close attention to the drug production in the region,