U.S. Food and Drug Administration
The FDA is responsible for protecting the public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, and medical devices; and by …
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FDA Industry Systems
2023年10月31日 · FDA Industry Systems (FIS) was created to facilitate making submissions to the U.S. Food and Drug Administration (FDA), including registrations, listings, and other …
MyPlate.gov | U.S. Department of Agriculture
MyPlate is the official symbol of the five food groups. Learn how to make MyPlate work for you. The Dietary Guidelines for Americans, 2020-2025 is available. Learn more. From MyPlate to …
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Electronic Submissions Gateway | FDA
The FDA ESG enables the secure submission of premarket and postmarket regulatory information for review. Refer to ESG's Center Submission Types webpage for the list of acceptable …
Registration and Listing | FDA
2023年7月7日 · Domestic and foreign establishments that manufacture, repack, or re-label drug products in the United States are required to register with the FDA. Domestic and foreign drug …
FDA Direct - Food and Drug Administration
CDER Direct allows users to easily create and submit data directly to the FDA. This system will provide information to FDA/CDER about drug manufacturers and private label distributors,...
WebTrader - Food and Drug Administration
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Log in | FDA
SSO Login for Drug Approvals and Databases Make sure to insert your PIV card into reader, before clicking above. Request Access Send to FDA OMUF Help