The United States Food and Drug Administration (FDA)
FDA Guidance and Regulatory Information
USER NOTICE for FDA Regulations and FDA Regulatory Information
Annual Edition for 21 CFR Food and Drugs Here.
The OFR updates the material in the e-CFR on a daily basis.
The current update status appears at the top of all e-CFR web pages. The Following e-CFR Data Is Current.
|Title||Volume||Chapter||Browse Parts||Regulatory Entity|
Food and Drugs
|1||I||1-99||Food and Drug Administration (FDA),
Department of Health and Human Services (DHHS)
|9||II||1300-1399||Drug Enforcement Administration,
Department of Justice
|III||1400-1499||Office of National Drug Control Policy|
The Electronic Code of Federal Regulations (e-CFR) is a currently updated version of the Code of Federal Regulations (CFR).
The e-CFR is an editorial compilation of CFR material and Federal Register amendments produced by the National Archives and Records Administration’s Office of the Federal Register (OFR) and the Government Printing Office.
About FDA Guidance Net
We freely share and provide healthcare, regulatory and medical information announced, issued or published by the United States Food and Drug Administration (US FDA), striving to help the industry, consumers and the public get better informed with practical information.
Areas of FDA Information
We provide FDA information in many areas, including the following, but not limited to.
- Combination products
- Medical devices
- In vitro diagnostic products
- Blood and vaccine products
- Clinical information
- Animal food and drugs
- FDA inspection and enforcement actions
- FDA warning letters
- Consent decree (permanent injunction)
DISCLAIMER: The information on this website is to increase our readers’ awareness and for information and sharing purposes only and should not be considered or construed as “medical advice” in any way, shape, form or manner.
Last Updated: 2016-06-06