Meetings, Conferences, & Workshops(CDER组织的会议和研讨会)、CDER Learn Training and Education(CDER组织的培训学习和继续教育机会)、Notable Approvals | Drugs(值得关注的人体药物批准进展)、New Drugs at FDA(FDA审批通过的新药产品)、Advisory Committee Calendar(咨询委员会日程)、T...
Updates, News, Events, and Training(新的审评进展、新产品和新培训课程): 这个模块共包括Recent New and Generic Drug Approvals(近期新药和仿制药批准进展)、Meetings, Conferences, & Workshops(CDER组织的会议和研讨会)、CDER Learn Training and Education(CDER组织的培训学习和继续教育机会)、Notable Approvals...
点击Updates, News, Events, and Training,出现下方界面,共包括Recent New and Generic Drug Approvals(近期新药和仿制药批准进展)、Meetings, Conferences, & Workshops(CDER组织的会议和研讨会)、CDER Learn Training and Education(CDER组织的培训学习和继续教育机会)、Notable Approvals | Drugs(值得关注的人体药物批...
点击Updates, News, Events, and Training,出现下方界面,共包括Recent New and Generic Drug Approvals(近期新药和仿制药批准进展)、Meetings, Conferences, & Workshops(CDER组织的会议和研讨会)、CDER Learn Training and Education(CDER组织的培训学习和继续教育机会)、Notable Approvals | Drugs(值得关注的人体药物批...
Workshops & Conferences (Medical Devices) - FDA/CDRH Public Meeting: Oversight of Laboratory Developed Tests (LDTs), Date July 19-20, 2010 来自 fda.gov 喜欢 0 阅读量: 46 被引量: 5 收藏 引用 批量引用 报错 分享 全部来源 求助全文 fda.gov 参考文献 引证文献...
⑨ Past Meetings, Conferences, & Workshops (会议和研讨会) (强烈推荐) FDA评审专家每年会参加很多会议和研讨会等,涉及的会议话题包括药物各层面,他们会解读最新FDA观点,并在会后由FDA将这些会议的PPT上传至网站,可以根据时间及内容进行搜索。其实这一点和国内的’药融圈’平台一样,通过邀请国内专家大咖分析国内医...
法规要求，保障申报产品的合规性。十六、最新审评进展与培训资源 提供Recent New and Generic Drug Approvals、Meetings, Conferences, & Workshops等板块，让广大药物工作者随时掌握行业动态。同时，CDER Learn Training and Education板块提供丰富的培训资源，覆盖多个领域，满足不同用户的需求。
Invites applications for the financial support of small scientific conferences and workshops in the United States from the Food and Drug Administration. Deadline of application; Amount of grant; Eligibility to the program; Support for meetings related to the agency's health and regulatory missions....
5. FDA孤儿药认定趋势和2022年上半年情况深度分析。https://mp.weixin.qq.com/s/WqSohWN6r6u5rw7ClSD18g 信息来源: [1] Public meeting: FDA Rare Disease Day 2023. https://www.fda.gov/news-events/fda-meetings-conferences-and-workshops/public-meeting-fda-rare-disease-day-2023-02272023...
FDA 483 指导手册说明书 Guide for US FDA-Regulated Organizations “How to Respond to (and Avoid) FDA Form 483s for Temperature, Humidity and other Controlled Environments”By Ken Appel, VP of Regulated Markets Veriteq, a Vaisala company ...