论文部分内容阅读
为进一步规范健康相关产品卫生行政许可工作,卫生部依据《中华人民共和国行政许可法》和《卫生行政许可管理办法》,组织制定了《健康相关产品卫生行政许可程序》(以下简称《程序》),同时发布了与之配套的相关文件,并于2006年6月1日起实行。新法规颁布后,引起业内普遍关注。为此,我们邀请了卫生部卫生监督中心吴建军处长对相关问题进行解答。
In order to further regulate health administrative licensing of health-related products, the Ministry of Health has organized and formulated the “Procedures for Health Administrative Licensing of Health-Related Products” (hereinafter referred to as the “Procedures”) in accordance with the Administrative Licensing Law of the People’s Republic of China and the Administrative Measures on Health Administrative Licensing At the same time, the related documents were released and implemented on June 1, 2006. After the promulgation of new laws and regulations, aroused widespread concern in the industry. To this end, we invited Wu Jianjun, director of the Health Inspection Center of the Ministry of Health, to answer relevant questions.