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Regulatory Information
Electronic Reading Room
This index contains categories of frequently requested FDA documents. Before submitting an FOIA request, please check to see if the records you seek are already available on an FDA Web site. You can use this index to locate a specific category of documents. In addition, you can check specific FOI sites which have been established by the following agency offices:
CATEGORIES OF DOCUMENTS
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Center for Drug Evaluation and Research (CDER)
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Center for Devices and Radiological Health (CDRH)
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Center for Veterinary Medicine (CVM)
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Office of Regulatory Affairs (ORA)
- ORA FOIA Electronic Reading Room
- Office of Regulatory Affairs
- Guide to International Inspection and Travel
- Inspection Guides
- Disqualified/Restricted/ Restrictions Removed/ Assurance Lists for Clinical Investigators
- Commissioning
- FDA Public Affairs Specialists
- Import Alerts
- FDA Debarment List
- Import Refusals
- Inspection Technical Guides
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Frequently Requested Regulatory Records
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