受国际知名专业机构汤森路透（Thomson Reuters）邀请，环球律师事务所为其全球法律实务指南系列（Practical Law Series）撰写Medical Devices: Sources of Regulation in China篇章，该篇章已于近期正式发布。汤森路透致力于为全球律师提供一流的法律实务知识，其法律实务指南中涉及不同国家和地区的篇章均由其邀请该专业领域广受认可的律师及团队所撰写。

Thomson Reuters, one of the most authoritative international legal agencies, invited Global Law Office and team to contribute to the Medical Devices: Sources of Regulation in China, Practical Law Series. Each Practical Law Series chapter has been exclusively contributed by lawyers from leading firms who are widely recognized in the practice area, providing first-class legal practice knowledge for lawyers around the world.

此次Medical Devices: Sources of Regulation in China篇章由环球律师事务所周磊、范可撰写，着重介绍了中国法律下的医疗器械及消费者健康产品适用的产品安全监管制度、商业化和产品生命周期管理、对医疗器械及消费者健康产品的监管与执法、有关责任和相关政策及立法趋势等内容，希望可以为读者了解中国法律对医疗器械及消费者健康产品的监管提供全面、系统、权威的法律实务指南。如果您希望就本指南或者与本指南讨论的内容进一步交流，敬请联系撰文作者。

The Medical Devices: Sources of Regulation in China is written by legal professionals of Global Law Office, Alan Zhou and Coco Fan. The aritlce provides an overview of the regulatory administration and enforcement on medical devices and consumer health products, the commercialisation and product life cycle management, related liabilities as well as relevant policy and legislative trends applicable to medical devices and consumer health products under the PRC law, aiming to provide enterprises with a more comprehensive perspective to understand the supervision and administration of medical devices and consumer health products in China. Should you have inquiries or comment regarding the publication, please feel free to contact the authors.

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