food-and-drug-administration

Documents about food-and-drug-administration

• 21 CFR Part 820 — Quality Management System Regulation#506893Code of Federal Regulations (eCFR)
• 21 CFR Part 821 — Medical Device Tracking Requirements#506894Code of Federal Regulations (eCFR)
• 21 CFR Part 860 — Medical Device Classification Procedures#506897Code of Federal Regulations (eCFR)
• 21 CFR Part 1005 — Importation of Electronic Products#506922Code of Federal Regulations (eCFR)
• 21 CFR Part 1114 — Premarket Tobacco Product Applications#506930Code of Federal Regulations (eCFR)
• 21 CFR Part 1143 — Minimum Required Warning Statements#506933Code of Federal Regulations (eCFR)
• 21 CFR Part 112 — Standards for the Growing, Harvesting, Packing, and Holding of Produce for Human Consumption#506741Code of Federal Regulations (eCFR)
• 21 CFR Part 500 — General#506843Code of Federal Regulations (eCFR)
• 21 CFR Part 874 — Ear, Nose, and Throat Devices#506905Code of Federal Regulations (eCFR)
• 21 CFR Part 878 — General and Plastic Surgery Devices#506907Code of Federal Regulations (eCFR)
• 21 CFR Part 710 — Voluntary Registration of Cosmetic Product Establishments#506880Code of Federal Regulations (eCFR)
• 21 CFR Part 814 — Premarket Approval of Medical Devices#506892Code of Federal Regulations (eCFR)
• 21 CFR Part 861 — Procedures for Performance Standards Development#506898Code of Federal Regulations (eCFR)
• United States Food and Drug Administration Approval of Neurosurgical Devices: A 25-Year Review of Non-510(k) Pathway Trends#657819Cornell eCommons
• 21 CFR Part 579 — Irradiation in the Production, Processing, and Handling of Animal Feed and Pet Food#506865Code of Federal Regulations (eCFR)
• 21 CFR Part 19 — Standards of Conduct and Conflicts of Interest#506713Code of Federal Regulations (eCFR)
• 21 CFR Part 299 — Drugs; Official Names and Established Names#506810Code of Federal Regulations (eCFR)
• 21 CFR Part 320 — Bioavailability and Bioequivalence Requirements#506818Code of Federal Regulations (eCFR)
• 21 CFR Part 862 — Clinical Chemistry and Clinical Toxicology Devices#506899Code of Federal Regulations (eCFR)
• 21 CFR Part 880 — General Hospital and Personal Use Devices#506908Code of Federal Regulations (eCFR)
• 21 CFR Part 1107 — Exemption Requests and Substantial Equivalence Reports#506929Code of Federal Regulations (eCFR)
• 21 CFR Part 111 — Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements#506740Code of Federal Regulations (eCFR)
• 21 CFR Part 14 — Public Hearing Before a Public Advisory Committee#506709Code of Federal Regulations (eCFR)
• 21 CFR Part 58 — Good Laboratory Practice for Nonclinical Laboratory Studies#506720Code of Federal Regulations (eCFR)
• 21 CFR Part 73 — Listing of Color Additives Exempt from Certification#506724Code of Federal Regulations (eCFR)
• 21 CFR Part 74 — Listing of Color Additives Subject to Certification#506725Code of Federal Regulations (eCFR)
• 21 CFR Part 250 — Special Requirements for Specific Human Drugs#506807Code of Federal Regulations (eCFR)
• 21 CFR Part 1010 — Performance Standards for Electronic Products: General#506923Code of Federal Regulations (eCFR)
• 21 CFR Part 1040 — Performance Standards for Light-Emitting Products#506926Code of Federal Regulations (eCFR)
• 21 CFR Part 82 — Listing of Certified Provisionally Listed Colors and Specifications#506728Code of Federal Regulations (eCFR)
• 21 CFR Part 510 — New Animal Drugs#506848Code of Federal Regulations (eCFR)
• 21 CFR Part 640 — Additional Standards for Human Blood and Blood Products#506875Code of Federal Regulations (eCFR)
• 21 CFR Part 806 — Medical Devices; Reports of Corrections and Removals#506886Code of Federal Regulations (eCFR)
• 21 CFR Part 1140 — Cigarettes, Smokeless Tobacco, and Covered Tobacco Products#506931Code of Federal Regulations (eCFR)
• 21 CFR Part 1141 — Required Warnings for Cigarette Packages and Advertisements#506932Code of Federal Regulations (eCFR)
• 21 CFR Part 13 — Public Hearing Before a Public Board of Inquiry#506708Code of Federal Regulations (eCFR)
• 21 CFR Part 211 — Current Good Manufacturing Practice for Finished Pharmaceuticals#506800Code of Federal Regulations (eCFR)
• 21 CFR Part 213 — Current Good Manufacturing Practice for Medical Gases#506802Code of Federal Regulations (eCFR)
• 21 CFR Part 225 — Current Good Manufacturing Practice for Medicated Feeds#506804Code of Federal Regulations (eCFR)
• 21 CFR Part 660 — Additional Standards for Diagnostic Substances for Laboratory Tests#506876Code of Federal Regulations (eCFR)
• 21 CFR Part 720 — Voluntary Filing of Cosmetic Product Ingredient Composition Statements#506881Code of Federal Regulations (eCFR)
• 21 CFR Part 809 — In Vitro Diagnostic Products for Human Use#506889Code of Federal Regulations (eCFR)
• 21 CFR Part 1003 — Notification of Defects or Failure to Comply#506920Code of Federal Regulations (eCFR)
• 21 CFR Part 1004 — Repurchase, Repairs, or Replacement of Electronic Products#506921Code of Federal Regulations (eCFR)
• 21 CFR Part 1020 — Performance Standards for Ionizing Radiation Emitting Products#506924Code of Federal Regulations (eCFR)
• 21 CFR Part 507 — Current Good Manufacturing Practice, Hazard Analysis, and Risk-Based Preventive Controls for Food for Animals#506846Code of Federal Regulations (eCFR)
• 21 CFR Part 584 — Food Substances Affirmed as Generally Recognized as Safe in Feed and Drinking Water of Animals#506867Code of Federal Regulations (eCFR)
• 21 CFR Part 230 — Certification and Postmarketing Reporting for Designated Medical Gases#506806Code of Federal Regulations (eCFR)
• 21 CFR Part 515 — Medicated Feed Mill License#506851Code of Federal Regulations (eCFR)
• 21 CFR Part 606 — Current Good Manufacturing Practice for Blood and Blood Components#506871Code of Federal Regulations (eCFR)