food-and-drug-administration

Documents about food-and-drug-administration

• AI-Enabled Optimization of Early-Phase Clinical Trials Pilot Program; Request for Information#512183Federal Register
• 21 CFR Part 528 — Intentional Genomic Alterations in Animals#506857Code of Federal Regulations (eCFR)
• 21 CFR Part 582 — Substances Generally Recognized as Safe#506866Code of Federal Regulations (eCFR)
• 21 CFR Part 898 — Performance Standard for Electrode Lead Wires and Patient Cables#506916Code of Federal Regulations (eCFR)
• 21 CFR Part 1030 — Performance Standards for Microwave and Radio Frequency Emitting Products#506925Code of Federal Regulations (eCFR)
• 21 CFR Part 106 — Infant Formula Requirements Pertaining to Current Good Manufacturing Practice, Quality Control Procedures, Quality Factors, Records and Reports, and Notifications#506735Code of Federal Regulations (eCFR)
• UC Comments on Certificates of Confidentiality; Draft Guidance for Sponsors, Sponsor-Investigators, Researchers, Industry, and Food and Drug Administration Staff: Availability (FDA-2019-D-3592)#629368eScholarship
• 21 CFR Part 212 — Current Good Manufacturing Practice for Positron Emission Tomography Drugs#506801Code of Federal Regulations (eCFR)
• 21 CFR Part 226 — Current Good Manufacturing Practice for Type a Medicated Articles#506805Code of Federal Regulations (eCFR)
• 21 CFR Part 511 — New Animal Drugs for Investigational Use#506849Code of Federal Regulations (eCFR)
• 21 CFR Part 520 — Oral Dosage Form New Animal Drugs#506853Code of Federal Regulations (eCFR)
• 21 CFR Part 526 — Intramammary Dosage Form New Animal Drugs#506856Code of Federal Regulations (eCFR)
• 21 CFR Part 207 — Requirements for Foreign and Domestic Establishment Registration and Listing for Human Drugs, Including Drugs That Are Regulated Under a Biologics License Application, and Animal Drugs, and the National Drug Code#506796Code of Federal Regulations (eCFR)
• 21 CFR Part 332 — Antiflatulent Products for Over-the-Counter Human Use#506823Code of Federal Regulations (eCFR)
• 21 CFR Part 529 — Certain Other Dosage Form New Animal Drugs#506858Code of Federal Regulations (eCFR)
• 21 CFR Part 808 — Exemptions from Federal Preemption of State and Local Medical Device Requirements#506888Code of Federal Regulations (eCFR)
• 21 CFR Part 524 — Ophthalmic and Topical Dosage Form New Animal Drugs#506855Code of Federal Regulations (eCFR)
• 21 CFR Part 807 — Establishment Registration and Device Listing for Manufacturers and Initial Importers of Devices#506887Code of Federal Regulations (eCFR)
• 21 CFR Part 331 — Antacid Products for Over-the-Counter (OTC) Human Use#506822Code of Federal Regulations (eCFR)
• 21 CFR Part 99 — Dissemination of Information on Unapproved/New Uses for Marketed Drugs, Biologics, and Devices#506729Code of Federal Regulations (eCFR)
• 21 CFR Part 209 — Requirement for Authorized Dispensers and Pharmacies to Distribute a Side Effects Statement#506798Code of Federal Regulations (eCFR)
• 21 CFR Part 502 — Common or Usual Names for Nonstandardized Animal Foods#506845Code of Federal Regulations (eCFR)
• 21 CFR Part 522 — Implantation or Injectable Dosage Form New Animal Drugs#506854Code of Federal Regulations (eCFR)
• 21 CFR Part 558 — New Animal Drugs for Use in Animal Feeds#506861Code of Federal Regulations (eCFR)
• 21 CFR Part 516 — New Animal Drugs for Minor Use and Minor Species#506852Code of Federal Regulations (eCFR)
• 21 CFR Part 1300 — Definitions#506940Code of Federal Regulations (eCFR)
• 21 CFR Part 1303 — Quotas#506943Code of Federal Regulations (eCFR)
• 21 CFR Part 1306 — Prescriptions#506946Code of Federal Regulations (eCFR)
• 21 CFR Part 1307 — Miscellaneous#506947Code of Federal Regulations (eCFR)
• 21 CFR Part 1317 — Disposal#506957Code of Federal Regulations (eCFR)
• 21 CFR Part 630 — Requirements for Blood and Blood Components Intended for Transfusion or for Further Manufacturing Use#506874Code of Federal Regulations (eCFR)
• 21 CFR Part 210 — Current Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs; General#506799Code of Federal Regulations (eCFR)
• 21 CFR Part 607 — Establishment Registration and Product Listing for Manufacturers of Human Blood and Blood Products and Licensed Devices#506872Code of Federal Regulations (eCFR)
• The Influence of Different Food Componente on Zinc Absorption in Young Adults Consuming Zinc Fortified Porridges Prepared From Maize, Beans and Sorghum: a Series of Six Similar Randomized, Single-blind Studies#866188ClinicalTrials.gov
• 21 CFR Part 81 — General Specifications and General Restrictions for Provisional Color Additives for Use in Foods, Drugs, and Cosmetics#506727Code of Federal Regulations (eCFR)
• 21 CFR Part 369 — Interpretative Statements Re Warnings on Drugs and Devices for Over-the-Counter Sale#506842Code of Federal Regulations (eCFR)
• 21 CFR Part 1321 — DEA Mailing Addresses#506959Code of Federal Regulations (eCFR)
• 21 CFR Part 1304 — Records and Reports of Registrants#506944Code of Federal Regulations (eCFR)
• 21 CFR Part 1316 — Administrative Functions, Practices, and Procedures#506956Code of Federal Regulations (eCFR)
• 21 CFR Part 1308 — Schedules of Controlled Substances#506948Code of Federal Regulations (eCFR)
• 21 CFR Part 1311 — Requirements for Electronic Orders and Prescriptions#506951Code of Federal Regulations (eCFR)
• 21 CFR Part 1312 — Importation and Exportation of Controlled Substances#506952Code of Federal Regulations (eCFR)
• 21 CFR Part 330 — Over-the-Counter (OTC) Human Drugs Which Are Generally Recognized as Safe and Effective and Not Misbranded#506821Code of Federal Regulations (eCFR)
• 21 CFR Part 1302 — Labeling and Packaging Requirements for Controlled Substances#506942Code of Federal Regulations (eCFR)
• 21 CFR Part 361 — Prescription Drugs for Human Use Generally Recognized as Safe and Effective and Not Misbranded: Drugs Used in Research#506841Code of Federal Regulations (eCFR)
• 21 CFR Part 1305 — Orders for Schedule I and II Controlled Substances#506945Code of Federal Regulations (eCFR)
• 21 CFR Part 1315 — Importation and Production Quotas for Ephedrine, Pseudoephedrine, and Phenylpropanolamine#506955Code of Federal Regulations (eCFR)
• 21 CFR Part 1314 — Retail Sale of Scheduled Listed Chemical Products#506954Code of Federal Regulations (eCFR)
• 21 CFR Part 1301 — Registration of Manufacturers, Distributors, and Dispensers of Controlled Substances#506941Code of Federal Regulations (eCFR)
• 21 CFR Part 1313 — Importation and Exportation of List I and List II Chemicals#506953Code of Federal Regulations (eCFR)