• CFR 21(PTS1-99) : 2019

    Superseded A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

    Code of Federal Regulations, Title 21, Food and Drugs, Part 1-99, Revised as of April 1, 2019

    Available format(s):  Hardcopy

    Superseded date:  24-12-2021

    Language(s):  English

    Published date:  24-10-2019

    Publisher:  Code of Federal Regulations

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    Table of Contents - (Show below) - (Hide below)

    1
    1.1 to 1.980
    GENERAL ENFORCEMENT REGULATIONS
    2
    2.5 to 2.125
    GENERAL ADMINISTRATIVE RULINGS AND DECISIONS
    3
    3.1 to 3.10
    PRODUCT JURISDICTION
    4
    4.1 to 4.105
    REGULATION OF COMBINATION PRODUCTS
    5
    5.1100 to 5.1110
    ORGANIZATION
    7
    7.1 to 7.87
    ENFORCEMENT POLICY
    10
    10.1 to 10.206
    ADMINISTRATIVE PRACTICES AND PROCEDURES
    11
    11.1 to 11.300
    ELECTRONIC RECORDS; ELECTRONIC SIGNATURES
    12
    12.1 to 12.159
    FORMAL EVIDENTIARY PUBLIC HEARING
    13
    13.1 to 13.50
    PUBLIC HEARING BEFORE A PUBLIC BOARD OF INQUIRY
    14
    14.1 to 14.174
    PUBLIC HEARING BEFORE A PUBLIC ADVISORY COMMITTEE
    15
    15.1 to 15.45
    PUBLIC HEARING BEFORE THE COMMISSIONER
    16
    16.1 to 16.120
    REGULATORY HEARING BEFORE THE FOOD AND DRUG ADMINISTRATION
    17
    17.1 to 17.54
    CIVIL MONEY PENALTIES HEARINGS
    19
    19.1 to 19.55
    STANDARDS OF CONDUCT AND CONFLICTS OF INTEREST
    20
    20.1 to 20.120
    PUBLIC INFORMATION
    21
    21.1 to 21.75
    PROTECTION OF PRIVACY
    25
    25.1 to 25.60
    ENVIRONMENTAL IMPACT CONSIDERATIONS
    26
    26.0 to 26.81
    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
    50
    50.1 to 50.56
    PROTECTION OF HUMAN SUBJECTS
    54
    54.1 to 54.6
    FINANCIAL DISCLOSURE BY CLINICAL INVESTIGATORS
    56
    56.101 to 56.124
    INSTITUTIONAL REVIEW BOARDS
    58
    58.1 to 58.219
    GOOD LABORATORY PRACTICE FOR NONCLINICAL LABORATORY STUDIES
    60
    60.1 to 60.46
    PATENT TERM RESTORATION
    70
    70.3 to 70.55
    COLOR ADDITIVES
    71
    71.1 to 71.37
    COLOR ADDITIVE PETITIONS
    73
    73.1 to 73.3129
    LISTING OF COLOR ADDITIVES EXEMPT FROM CERTIFICATION
    74
    74.101 to 74.3710
    LISTING OF COLOR ADDITIVES SUBJECT TO CERTIFICATION
    80
    80.10 to 80.39
    COLOR ADDITIVE CERTIFICATION
    81
    81.1 to 81.32
    GENERAL SPECIFICATIONS AND GENERAL RESTRICTIONS FOR PROVISIONAL COLOR ADDITIVES FOR USE IN FOODS, DRUGS, AND COSMETICS
    82
    82.3 to 82.2707a
    LISTING OF CERTIFIED PROVISIONALLY LISTED COLORS AND SPECIFICATIONS
    83-98
    [RESERVED]
    99
    99.1 to 99.501
    DISSEMINATION OF INFORMATION ON UNAPPROVED/NEW USES FOR MARKETED DRUGS, BIOLOGICS, AND DEVICES

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    Document Type Regulation
    Publisher Code of Federal Regulations
    Status Superseded
    Superseded By
    Supersedes
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