The Food and Drug Administration (FDA) is the agency of the United States that regulates and supervises food, tobacco, drugs, cosmetics, medical devices, vaccines, biopharmaceuticals, radiation emitting devices, and veterinary products. It also deals with promoting and protecting public health by encouraging innovation and providing accurate information to the public about improving their health.
The FDA is run by the Commissioner of Food and Drugs, a person appointed by the President, advised by the Senate, and reporting to the Secretary of Health and Human Services. The agency is run by the United States Department of Health and Human Services, a federal executive department of the United States
The Center for Devices and Radiological Health (CDRH) is the department that deals with premarket approval for medical devices, as well as supervises the safety, manufacturing, and performance of the devices.
The structure of the Center for Devices and Radiological Health:
A list of FDA regulations can be found here on our website.
自2018年起,美国食品和药物管理局(U.S. Food and Drug Administration,FDA)开始试行以电子化方式来帮助行业提供完整的510(k)上市前通知。2022年,为推进以电子格式提供510(k)递交文件的过渡,美国FDA正式发布关于使用电子递交模板和资源的最终指导文
阅读更多我们的专家将详细解读2023年韩国食品药品安全部(MFDS)指导文件草案更新下韩国医疗器械注册监管要求、分类标准、韩国良好生产规范(KGMP)等相关要求,并将依据多年韩国本地注册经验提供注册案例分享。此外,您还将了解到制造商在面对MFDS监管时需要关注的核心要点,相关研讨会内容包括:
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