世卫将辉瑞和BioNTech研发的新冠疫苗列为可紧急使用。
世卫组织决定，将美国辉瑞大药厂（Pfizer）和德国生技公司BioNTech合力研制的新冠疫苗，列为可用于紧急用途，期望为各国加快批准进口和注射疫苗开启大门。
世卫指，审查发现辉瑞与BioNTech疫苗符合世卫设定不可或缺的安全和有效标准，使用该疫苗的好处抵销了潜在风险。
同时强调，全球要投入更大努力，确保有足够疫苗供应，满足各地高危群组需要。现时这款疫苗已获得英国、欧盟药品管理局（EMA）、美国食品暨药物管理局、加拿大卫生部、巴林、以色列、科威特、墨西哥和新加坡等的监管当局支持。
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