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
USA List Price:
$45.00 Display International Price
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In Stock
GPO Stock Number: 869-084-00067-1 ISBN: 9780160932694
Price: $45.00

Description

Code of Federal Regulations, Title 21, Food and Drugs, Parts 1-99 covers rules, regulations, and procedures relating to the Food and Drug Administration and the Department of Health and Human Services. This volume includes general enforcement regulations, enforcement policy, civil money penalties hearings, protection of human subjects, and more.

TABLE OF CONTENTS

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

Subchapter A - GENERAL (Parts 1 - 99)
Part 1 - GENERAL ENFORCEMENT REGULATIONS
Part 2 - GENERAL ADMINISTRATIVE RULINGS AND DECISIONS
Part 3 - PRODUCT JURISDICTION
Part 4 - REGULATION OF COMBINATION PRODUCTS
Part 5 - ORGANIZATION
Part 7 - ENFORCEMENT POLICY
Part 10 - ADMINISTRATIVE PRACTICES AND PROCEDURES
Part 11 - ELECTRONIC RECORDS; ELECTRONIC SIGNATURES
Part 12 - FORMAL EVIDENTIARY PUBLIC HEARING
Part 13 - PUBLIC HEARING BEFORE A PUBLIC BOARD OF INQUIRY
Part 14 - PUBLIC HEARING BEFORE A PUBLIC ADVISORY COMMITTEE
Part 15 - PUBLIC HEARING BEFORE THE COMMISSIONER
Part 16 - REGULATORY HEARING BEFORE THE FOOD AND DRUG ADMINISTRATION
Part 17 - CIVIL MONEY PENALTIES HEARINGS
Part 19 - STANDARDS OF CONDUCT AND CONFLICTS OF INTEREST
Part 20 - PUBLIC INFORMATION
Part 21 - PROTECTION OF PRIVACY
Part 25 - ENVIRONMENTAL IMPACT CONSIDERATIONS
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
Part 50 - PROTECTION OF HUMAN SUBJECTS
Part 54 - FINANCIAL DISCLOSURE BY CLINICAL INVESTIGATORS
Part 56 - INSTITUTIONAL REVIEW BOARDS
Part 58 - GOOD LABORATORY PRACTICE FOR NONCLINICAL LABORATORY STUDIES
Part 60 - PATENT TERM RESTORATION
Part 70 - COLOR ADDITIVES
Part 71 - COLOR ADDITIVE PETITIONS
Part 73 - LISTING OF COLOR ADDITIVES EXEMPT FROM CERTIFICATION
Part 74 - LISTING OF COLOR ADDITIVES SUBJECT TO CERTIFICATION
Part 80 - COLOR ADDITIVE CERTIFICATION
Part 81 - GENERAL SPECIFICATIONS AND GENERAL RESTRICTIONS FOR PROVISIONAL COLOR ADDITIVES FOR USE IN FOODS, DRUGS, AND COSMETICS
Part 82 - LISTING OF CERTIFIED PROVISIONALLY LISTED COLORS AND SPECIFICATIONS
Parts 83-98 - Reserved
Part 99 - DISSEMINATION OF INFORMATION ON UNAPPROVED/NEW USES FOR MARKETED DRUGS, BIOLOGICS, AND DEVICES

Audience: This volume would be of importance to food, pharmaceutical, and cosmetic manufacturers. In addition, Food and Drug Administration and Health and Human Services personnel may be interested in this volume.

Keywords: Code of Federal Regulations Title 21, code of federal regulations title 21, CFR Title 21, cfr title 21, Food and Drug Administration, FDA, food and drug administration, Health and Human Services, HHS, drugs, pharmaceuticals, food and drugs, cosmetics, FDA regulations

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:
06/10/2016
Last Status Update:
06/02/2017