T 21 Pts 1-99; Code Of Federal Regulations Microfiche 2018

T 21 Pts 1-99; Code Of Federal Regulations Microfiche 2018
Title:
Code of Federal Regulations, Title 21, Food and Drugs, Pt. 1-99, Revised as of April 1, 2018 (Microfiche)
Format:
Microfiche
USA Price: 
Stock:
Low stock
GPO Stock Number:
869-087-00061-1
Description

21 CFR, Pt. 1-99, includes rules, regulations, procedures and administrative procedures associated with TITLE 21—Food and Drugs, CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES, SUBCHAPTER A—GENERAL

Table of Contents

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

Audience

Lawyers, law librarians and law students should be familiar with the Code of Federal Regulations. Law libraries and some academic libraries should have a copy of this publication for their patrons. In addition, members of government and policymakers, members of Congress, tax preparers, investment counselors and brokers, social activists, political consultants, media writers and producers, university instructors and professors, political scientists, and taxpayers would find this publication useful.

Product Details

Availability Details:
In Stock
USA Price:
$4.00
International Price:
$5.60
Publisher:
National Archives and Records Administration, Office of the Federal Register
Key Phrases:
  • CFR Title 21
Weight:
0.125
Quantity Price:
No Discount
Unit of Issue (US):
1
Unit of Issue (Non-US):
1
Record Creation Date:
10/26/2018
Last Status Update:
11/05/2018
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