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卫生部药政局于1988年2月28日～3月3日在北京中国检定所召开了国家级药品、生物制品监督员首次工作会议.卫生部药政局潘学田局长到会作了重要讲话,全体国家级药品、生物制品监督员及中国检定所张银如书记、邢文庭副所长、田颂九副书记等约40人参加了会议.会议期间,中国检定所质量情报处的杨景勋同志向全体代表介绍了世界各国GMP的开展情况以及国外监督员的工作情况;卫生部药政局王志清同志宣讲了中国药品管理法及其实
The Pharmaceutical Affairs Bureau of the Ministry of Health held the first working meeting of state-level drug and biological product supervisors at the Beijing China Accreditation Bureau from February 28 to March 3, 1988. Director Pan Xuetian of the State Council’s Pharmaceutical and Political Administration made an important speech at the meeting. Some 40 people, including state-level drug and biological product supervisors and China Inspector Zhang Yinru, Xing Wenting, deputy director Tian Shujiu, and other secretaries attended the meeting. During the meeting, Comrade Yang Jingxun, from the Quality Assurance Office of China’s accreditation body, introduced to all delegates The implementation of GMP in various countries in the world and the work of foreign supervisors; Comrade Wang Zhiqing of the Pharmaceutical Affairs Bureau of the Ministry of Health preached the Chinese Drug Administration Law and in fact