卫生总监丹斯里诺希山宣布,我国周二批准了中国制药公司康希诺(CanSino)和美国制药公司强生(Johnson & Johnson)的单剂新冠疫苗的有条件注册。
他今日(15日)发表声明说,卫生部药物监管局今日召开的第359次会议,批准了中国康希诺生物公司生产的克威莎疫苗( Convidecia Recombinant Novel Coronavirus Vaccine)以及美国强生推出的强生疫苗(Janssen COVID-19 Vaccine)的有条件注册。
他说,这两款疫苗皆属于只需要注射一剂的疫苗。
他说,强生疫苗已经获得世界卫生组织列入紧急使用清单,而我国政府这是通过全球冠病疫苗机制(COVAX)购买的强生疫苗。
他说,当局会不时根据最新数据来监督与评估这些获有条件批准的疫苗质量、安全性和有效性,以确保疫苗在收益与风险的比较中利大于弊。
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