Regulatory lessons from China’s COVID-19 vaccines development and approval policies

Jingshu Yang, Yue Yang
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引用次数: 2

Abstract

Coronavirus disease 2019, responsible for a global pandemic, is caused by the severe acute respiratory syndrome coronavirus 2. Several vaccines have been developed and approved worldwide, particularly in China. As of Oct 17, 2021, four new coronavirus vaccines in China have been conditionally approved for marketing by the National Medical Products Administration, two of which have been authorized for emergency use in the Emergency Use Listing of the World Health Organization. Domestic vaccine R&D in China has relied on legal and regulatory support. This article summarizes the regulatory policy for vaccine development, review and approval. Vaccine approval laws have been continually improved, and regulations for special approval have been used to shorten the review time. China has coordinated pandemic-related needs, both domestically and with other countries, and made substantial progress in cooperative international anti-pandemic efforts.
中国新冠肺炎疫苗研发和审批政策的监管经验教训
2019冠状病毒病是由严重急性呼吸系统综合征冠状病毒2引起的,是全球大流行的罪魁祸首。世界各地,特别是中国,已经开发并批准了几种疫苗。截至2021年10月17日,中国已有四种新型冠状病毒疫苗获得国家医疗产品管理局有条件批准上市,其中两种已在世界卫生组织的《紧急使用清单》中获得紧急使用授权。中国国内疫苗的研发依赖于法律和监管的支持。本文概述了疫苗开发、审查和批准的监管政策。疫苗审批法律不断完善,特别审批条例被用于缩短审查时间。中国协调了国内外疫情相关需求,在国际抗疫合作方面取得了实质性进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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