FDA US Commercial Drugs Manufacturers Directory Database(美国FDA的商品药材制造商数据集)数据摘要：The database contains the list of all drugs with commercial distribution in the US and the manufacturer name.中文关键词：计算机科学,医学,健康,FDA,商品药材制造商,英文关键词：Computer science,Medical,Health...
The US Food and Drug Administration (FDA) has announced that it will deactivate listing records in its database that have not been recently updated or certified, as required by regulation, or that include an establishment with an expired registration. "FDA regulations require all drug manufacturers...
KEYWORDS: Drug label; Database; Drugs@FDA; FDA Online Label Repository; DailyMed 总下载数: 81次 本日下载数: 2次 本月下载数: 81次 文件大小: 619.60Kb*注:未经本站明确许可,任何网站不得非法盗链资源下载连接及抄袭本站原创内容资源!在此感谢您的支持与合作!返回...
The U.S. Food and Drug Administration (FDA) 510(k) database is an essential resource maintained by the agency that holds records of premarket notifications, known as 510(k) submissions, which are required to demonstrate a medical device’s substantial equivalence to a device already legally mar...
美国FDA药品标签法规要求 U.S. Food and Drug Administration Notice: Archived Document The content in this document is provided on the FDA’s website for reference purposes only. It was current when produced, but is no longer maintained and may be outdated.
To facilitate preventing patient safety events, researchers have been using the Federal Drug Administration (FDA) Manufacturer and User Device Experience (MAUDE) database as a publicly accessible data source for retrieving reports of medical devices including Health Information Technology (HIT) devices. ...
(under section 510 of the Federal Food, Drug, and Cosmetic Act or section 351 of the Public Health Service Act), and those required to self-identify under GDUFA submit information separately to the respective systems. Each system p...
001 SYNTHROID LEVOTHYROXINE SODIUM TABLET;ORAL 0.025MG **See current Annual Edition, 1.8 Description of Special Situations, Levothyroxine Sodium Yes No AB1;AB2 2002/07/24 2002/07/24 Prescription 002 SYNTHROID LEVOTHYROXINE SODIUM TABLET;ORAL 0.05MG **See current Annual Edition, 1.8 Description of Sp...
(AAMI) is reporting that as part of efforts to keep track of devices throughout the supply chain, the Food and Drug Administration (FDA) has teamed up with the National Institutes of Health's National Library of Medicine to make data on unique device identifiers (UDI) publicly available ...
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