Tracy Teng女士现任美国FDA Registrar大中华区首席代表。2007年加入美国FDA Registrar,先后在其法国代表处和美国总部担任法规专员,2008年派往FDA Registrar驻华代表处任大中华区首席代表。她一直致力于对美国食品药品管理局(FDA)的法规研究,协助了超过5000家食品、医疗器械、药品和化妆品企业遵守美国FDA法规把产品打入美国市场。为政府机构、行业协会、贸易组织、物流协会、行业展会、亚马逊和阿里国际等跨界平台和相关政府部门做有关美国食品药品管理局(FDA)法规的讲演和培训。
Ms. Tracy Teng currently serves as the Chief Representative of the Greater China Region for Registrar Corp. She embarked on her journey with Registrar Corp in 2007 as a Compliance Specialist, dedicating herself to aiding companies in adhering to stringent U.S. Food and Drug Administration (FDA) requirements. Over the years, Tracy has delved deeply into US FDA regulations, providing invaluable support to over 5,000 enterprises exporting medical devices, food and beverages, cosmetics, and pharmaceuticals to the United States. Tracy has been an active educator, delivering insightful lectures and training sessions on FDA regulations to government agencies, industry associations, trade organizations, logistics associations, industry exhibitions, cross-border platforms such as Amazon and Alibaba International, and relevant governmental departments.
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| 日期 | 时间 | 会场 | Session | 角色 | 讲题 |
|---|---|---|---|---|---|
| 2026-05-30 | 08:55-09:10 | 分会场7(二层,N213会议室) |
中国眼科器械创新&生态建设与全球化发展论坛(下) |
讲者 | 美国FDA对医疗器械的上市路径和上市后监管要求 |
| 2026-05-30 | 09:40-10:10 | 分会场7(二层,N213会议室) |
中国眼科器械创新&生态建设与全球化发展论坛(下) |
嘉宾 | 圆桌讨论:中国眼科器械的“航海时代” |