Title 21

CHAPTER I

Chapter I - Food And Drug Administration, Department Of Health And Human Services

CHAPTER I - FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES

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