主要负责浙江省体外诊断试剂以及临检设备的技术审评工作，撰写《抗核抗体检测试剂注册技术审查指导原则》以及YY/T 1740.3《医用质谱仪 第3部分：电感耦合等离子体质谱仪》等多项国家指南和标准；担任浙江省医疗器械分类界定专家库成员、浙江省医疗器械创新服务联盟成员、浙江省和国家级医疗器械临床试验检查员。

Mainly responsible for the technical review of invitro diagnostic reagents and clinical laboratory equipment in Zhejiang Province. He has compiled multiple national guidelines and standards including the Guidelines for Technical Review of Registration of AntiNuclear Antibody Detection Reagents and YY/T 1740.3 Medical Mass Spectrometers — Part 3: Inductively Coupled Plasma Mass Spectrometers. He is a member of the expert database for medical device classification and definition, a member of the Zhejiang Medical Device Innovation Service Alliance, and a provincial and nationallevel medical device clinical trial inspector in Zhejiang Province.