Code of Federal Regulations, Title 21, Food and Drugs, Pt. 1-99, Revised as of A

Code of Federal Regulations, Title 21, Food and Drugs, Pt. 1-99, Revised as of April 1, 2016

Agency Publisher: National Archives and Records Administration, Office of the Federal Register
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In Stock
GPO Stock Number: 869-084-00067-1 ISBN: 9780160932694
Price: $45.00

Description

CFR Title 21,  Food and Drugs, includes rules, regulations, procedures, hearings, and adminstrative directives including,  general enforcement regulations, enforcement policy, civil money penalties hearings, protection of human subjects, and more...

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 4.4 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
 

Product Details

GPO Stock Number:
869-084-00067-1
ISBN:
9780160932694
Availability Details:
In Stock - Warehouse and Retail (Priced)
USA Price:
$45.00
International Price:
$63.00
Publisher:
National Archives and Records Administration, Office of the Federal Register
Author:
 
Year/Pages:
2016: 567 p.
Note:
 
Key Phrases:
CFR Title 21
SuDocs Class:
 
Weight:
1.375 lb.
Quantity Price:
Discount
Binding:
Paperback
Cover:
Paper
Subject Bibliography:
 
Unit of Issue (U.S.):
Each
Item Available Date:
06/09/2016
Last Status Update:
02/23/2017