FDA Regulations
by Jacob Kearns
The full text of FDA Food, Medical Device and Drug GMP regulations
| App Name | FDA Regulations |
|---|---|
| Developer | Jacob Kearns |
| Category | Business |
| Download Size | 4 MB |
| Latest Version | 1.20 |
| Average Rating | 4.56 |
| Rating Count | 162 |
| Google Play | Download |
| AppBrain | Download FDA Regulations Android app |
Note: This app does not represent a government entity, it is a copy and paste of regulations from the FDA.gov website.
This app contains the full content of the United States Food and Drug Administration (FDA) Food, Medical Device and Drug GMP Regulations. The following Title 21 Parts are included:
21CFR4: Regulation of Combination Products
21CFR11: Electronic Records: Electronic Signatures
21CFR108: Emergency Permit Control
21CFR110: Current Good Manufacturing Practice in Manufacturing, Packing or Holding Human Food
21CFR111: Current Good Manufacturing Practice in Manufacturing, Processing, Packing or Holding Operations for Dietary Supplements
21CFR113: Thermally Processed Low-Acid Foods Packaged in Hermetically Sealed Containers
21CFR114: Acidified Foods
21CFR117: Current Good Manufacturing Practice, Hazard Analysis, and Risk-Based Preventive Controls for Human Food
21CFR120: Hazard Analysis and Critical Control Point (HACCP) Systems
21CFR123: Fish and Fishery Products
21CFR210: Current Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs; General
21CFR211: Current Good Manufacturing Practice for Finished Pharmaceuticals
21CFR801: Labeling
21CFR803: Medical Device Reporting
21CFR806: Med Devices; Reports of Corrections & Removals
21CFR807: Establishment Registration
21CFR809: In Vitro Diagnostic Products
21CFR812: Investigational Device Exemptions
21CFR814: Premarket Approval of Medical Devices
21CFR820: Quality System Regulation
21CFR821: Medical Device Tracking Requirements
21CFR822: Postmarket Surveillance
21CFR830: Unique Device Identification
21CFR860: Classification Procedures
The FDA Food, Drug, and Medical Device regulations are split up by section, click on a section to expand that specific section. Click again to hide. Each section also contains a link to the FDA website which contains the regulation so you can verify that it is up to date.
The FDA regulations are stored on your device and don't require an internet connection to access.
This app is a useful for auditors and as a general reference, just keep your phone handy instead of carrying around a reference book.
Recent changes:
Update target apk.
This app contains the full content of the United States Food and Drug Administration (FDA) Food, Medical Device and Drug GMP Regulations. The following Title 21 Parts are included:
21CFR4: Regulation of Combination Products
21CFR11: Electronic Records: Electronic Signatures
21CFR108: Emergency Permit Control
21CFR110: Current Good Manufacturing Practice in Manufacturing, Packing or Holding Human Food
21CFR111: Current Good Manufacturing Practice in Manufacturing, Processing, Packing or Holding Operations for Dietary Supplements
21CFR113: Thermally Processed Low-Acid Foods Packaged in Hermetically Sealed Containers
21CFR114: Acidified Foods
21CFR117: Current Good Manufacturing Practice, Hazard Analysis, and Risk-Based Preventive Controls for Human Food
21CFR120: Hazard Analysis and Critical Control Point (HACCP) Systems
21CFR123: Fish and Fishery Products
21CFR210: Current Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs; General
21CFR211: Current Good Manufacturing Practice for Finished Pharmaceuticals
21CFR801: Labeling
21CFR803: Medical Device Reporting
21CFR806: Med Devices; Reports of Corrections & Removals
21CFR807: Establishment Registration
21CFR809: In Vitro Diagnostic Products
21CFR812: Investigational Device Exemptions
21CFR814: Premarket Approval of Medical Devices
21CFR820: Quality System Regulation
21CFR821: Medical Device Tracking Requirements
21CFR822: Postmarket Surveillance
21CFR830: Unique Device Identification
21CFR860: Classification Procedures
The FDA Food, Drug, and Medical Device regulations are split up by section, click on a section to expand that specific section. Click again to hide. Each section also contains a link to the FDA website which contains the regulation so you can verify that it is up to date.
The FDA regulations are stored on your device and don't require an internet connection to access.
This app is a useful for auditors and as a general reference, just keep your phone handy instead of carrying around a reference book.
Recent changes:
Update target apk.
