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 …
FDA Verification Portal - Food and Drug Administration
This online portal provides a comprehensive list of Establishments and Health Products with License to Operate (LTO) and Certificate of Product Registration/Notification (CPR/NN) …
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 …
Food and Drug Administration
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Send and Track Medical Device Premarket Submissions Online
2024年11月15日 · Track the progress of Premarket Approval (PMA) applications and PMA Panel-Track supplements in the CDRH Portal. Users can view their application status in near real …
Electronic Submissions Gateway | FDA
The FDA ESG enables the secure submission of premarket and postmarket regulatory information for review.
Import Program Tools | FDA
2024年10月9日 · FEI Portal (NEW) Look up a FDA Establishment Identifier (FEI) based on a firm name and address or validate an address of an FEI.
www.access.fda.gov
www.access.fda.gov
Sign In - Food and Drug Administration
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For Industry | FDA
Guidance, registration and listing, pay user fees, import programs, and more.
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