Title 21
Volume 1 CHAPTER I
Chapter I - Food And Drug Administration, Department Of Health And Human Services
| 21:1.0.1.1 | SUBCHAP A | SUBCHAPTER A - GENERAL | |
| 21:1.0.1.1.1 | PART 1 | PART 1 - GENERAL ENFORCEMENT REGULATIONS | |
| 21:1.0.1.1.1.7.32 | SUBJGRP 32 | General Provisions | |
| 21:1.0.1.1.1.7.33 | SUBJGRP 33 | Procedures for Registration of Food Facilities | |
| 21:1.0.1.1.1.7.34 | SUBJGRP 34 | Additional Provisions | |
| 21:1.0.1.1.1.8.35 | SUBJGRP 35 | General Provisions | |
| 21:1.0.1.1.1.8.36 | SUBJGRP 36 | Requirements To Submit Prior Notice of Imported Food | |
| 21:1.0.1.1.1.8.37 | SUBJGRP 37 | Consequences | |
| 21:1.0.1.1.1.9.38 | SUBJGRP 38 | General Provisions | |
| 21:1.0.1.1.1.9.39 | SUBJGRP 39 | Requirements for Nontransporters To Establish and Maintain Records To Identify the Nontransporter and Transporter Immediate Previous Sources of Food | |
| 21:1.0.1.1.1.9.40 | SUBJGRP 40 | Requirements for Nontransporters To Establish and Maintain Records To Identify the Nontransporter and Transporter Immediate Subsequent Recipients of Food | |
| 21:1.0.1.1.1.9.41 | SUBJGRP 41 | Requirements for Transporters To Establish and Maintain Records | |
| 21:1.0.1.1.1.9.42 | SUBJGRP 42 | General Requirements | |
| 21:1.0.1.1.1.9.43 | SUBJGRP 43 | Compliance Dates | |
| 21:1.0.1.1.1.10.44 | SUBJGRP 44 | General Provisions | |
| 21:1.0.1.1.1.10.45 | SUBJGRP 45 | How Does FDA Order a Detention | |
| 21:1.0.1.1.1.10.46 | SUBJGRP 46 | What Is the Appeal Process for a Detention Order | |
| 21:1.0.1.1.1.12.47 | SUBJGRP 47 | Recognition of Accreditation Bodies Under This Subpart | |
| 21:1.0.1.1.1.12.48 | SUBJGRP 48 | Requirements for Accreditation Bodies That Have Been Recognized Under This Subpart | |
| 21:1.0.1.1.1.12.49 | SUBJGRP 49 | Procedures for Recognition of Accreditation Bodies Under This Subpart | |
| 21:1.0.1.1.1.12.50 | SUBJGRP 50 | Accreditation of Third-Party Certification Bodies Under This Subpart | |
| 21:1.0.1.1.1.12.51 | SUBJGRP 51 | Requirements for Third-Party Certification Bodies That Have Been Accredited Under This Subpart | |
| 21:1.0.1.1.1.12.52 | SUBJGRP 52 | Procedures for Accreditation of Third-Party Certification Bodies Under This Subpart | |
| 21:1.0.1.1.1.12.53 | SUBJGRP 53 | Additional Procedures for Direct Accreditation of Third-Party Certification Bodies Under This Subpart | |
| 21:1.0.1.1.1.12.54 | SUBJGRP 54 | Requirements for Eligible Entities Under This Subpart | |
| 21:1.0.1.1.1.12.55 | SUBJGRP 55 | General Requirements of This Subpart | |
| 21:1.0.1.1.1.12.56 | SUBJGRP 56 | Requirements for User Fees Under This Subpart | |
| 21:1.0.1.1.1.14.57 | SUBJGRP 57 | General Provisions | |
| 21:1.0.1.1.1.14.58 | SUBJGRP 58 | Vehicles and Transportation Equipment | |
| 21:1.0.1.1.1.14.59 | SUBJGRP 59 | Transportation Operations | |
| 21:1.0.1.1.1.14.60 | SUBJGRP 60 | Training | |
| 21:1.0.1.1.1.14.61 | SUBJGRP 61 | Records | |
| 21:1.0.1.1.1.14.62 | SUBJGRP 62 | Waivers | |
| 21:1.0.1.1.2 | PART 2 | PART 2 - GENERAL ADMINISTRATIVE RULINGS AND DECISIONS | |
| 21:1.0.1.1.3 | PART 3 | PART 3 - PRODUCT JURISDICTION | |
| 21:1.0.1.1.4 | PART 4 | PART 4 - REGULATION OF COMBINATION PRODUCTS | |
| 21:1.0.1.1.5 | PART 5 | PART 5 - ORGANIZATION | |
| 21:1.0.1.1.6 | PART 6 | PART 6 - XXX | |
| 21:1.0.1.1.7 | PART 7 | PART 7 - ENFORCEMENT POLICY | |
| 21:1.0.1.1.8 | PART 10 | PART 10 - ADMINISTRATIVE PRACTICES AND PROCEDURES | |
| 21:1.0.1.1.9 | PART 11 | PART 11 - ELECTRONIC RECORDS; ELECTRONIC SIGNATURES | |
| 21:1.0.1.1.10 | PART 12 | PART 12 - FORMAL EVIDENTIARY PUBLIC HEARING | |
| 21:1.0.1.1.11 | PART 13 | PART 13 - PUBLIC HEARING BEFORE A PUBLIC BOARD OF INQUIRY | |
| 21:1.0.1.1.12 | PART 14 | PART 14 - PUBLIC HEARING BEFORE A PUBLIC ADVISORY COMMITTEE | |
| 21:1.0.1.1.13 | PART 15 | PART 15 - PUBLIC HEARING BEFORE THE COMMISSIONER | |
| 21:1.0.1.1.14 | PART 16 | PART 16 - REGULATORY HEARING BEFORE THE FOOD AND DRUG ADMINISTRATION | |
| 21:1.0.1.1.15 | PART 17 | PART 17 - CIVIL MONEY PENALTIES HEARINGS | |
| 21:1.0.1.1.16 | PART 19 | PART 19 - STANDARDS OF CONDUCT AND CONFLICTS OF INTEREST | |
| 21:1.0.1.1.17 | PART 20 | PART 20 - PUBLIC INFORMATION | |
| 21:1.0.1.1.18 | PART 21 | PART 21 - PROTECTION OF PRIVACY | |
| 21:1.0.1.1.19 | PART 25 | PART 25 - ENVIRONMENTAL IMPACT CONSIDERATIONS | |
| 21:1.0.1.1.20 | PART 26 | PART 26 - MUTUAL RECOGNITION OF PHARMACEUTICAL GOOD MANUFACTURING PRACTICE REPORTS, MEDICAL DEVICE QUALITY SYSTEM AUDIT REPORTS, AND CERTAIN MEDICAL DEVICE PRODUCT EVALUATION REPORTS: UNITED STATES AND THE EUROPEAN COMMUNITY | |
| 21:1.0.1.1.21 | PART 50 | PART 50 - PROTECTION OF HUMAN SUBJECTS | |
| 21:1.0.1.1.22 | PART 54 | PART 54 - FINANCIAL DISCLOSURE BY CLINICAL INVESTIGATORS | |
| 21:1.0.1.1.23 | PART 56 | PART 56 - INSTITUTIONAL REVIEW BOARDS | |
| 21:1.0.1.1.24 | PART 58 | PART 58 - GOOD LABORATORY PRACTICE FOR NONCLINICAL LABORATORY STUDIES | |
| 21:1.0.1.1.25 | PART 60 | PART 60 - PATENT TERM RESTORATION | |
| 21:1.0.1.1.26 | PART 70 | PART 70 - COLOR ADDITIVES | |
| 21:1.0.1.1.27 | PART 71 | PART 71 - COLOR ADDITIVE PETITIONS | |
| 21:1.0.1.1.28 | PART 73 | PART 73 - LISTING OF COLOR ADDITIVES EXEMPT FROM CERTIFICATION | |
| 21:1.0.1.1.29 | PART 74 | PART 74 - LISTING OF COLOR ADDITIVES SUBJECT TO CERTIFICATION | |
| 21:1.0.1.1.30 | PART 80 | PART 80 - COLOR ADDITIVE CERTIFICATION | |
| 21:1.0.1.1.31 | PART 81 | PART 81 - GENERAL SPECIFICATIONS AND GENERAL RESTRICTIONS FOR PROVISIONAL COLOR ADDITIVES FOR USE IN FOODS, DRUGS, AND COSMETICS | |
| 21:1.0.1.1.32 | PART 82 | PART 82 - LISTING OF CERTIFIED PROVISIONALLY LISTED COLORS AND SPECIFICATIONS | |
| 21:1.0.1.1.33 | PART 83-98 | PARTS 83-98 [RESERVED] | |
| 21:1.0.1.1.34 | PART 99 | PART 99 - DISSEMINATION OF INFORMATION ON UNAPPROVED/NEW USES FOR MARKETED DRUGS, BIOLOGICS, AND DEVICES |