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Cfr 21, Parts 1 To 99, Food And Drugs, April 01, 2016 (volume 1 Of 9) [Paperback]

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  • Category: Books (Law)
  • ISBN-10:  1359980180
  • ISBN-10:  1359980180
  • ISBN-13:  9781359980182
  • ISBN-13:  9781359980182
  • Publisher:  Regulations Press
  • Publisher:  Regulations Press
  • Pages:  568
  • Pages:  568
  • Binding:  Paperback
  • Binding:  Paperback
  • Pub Date:  01-Jun-2016
  • Pub Date:  01-Jun-2016
  • SKU:  1359980180-11-MPOD
  • SKU:  1359980180-11-MPOD
  • Item ID: 100735303
  • Seller: ShopSpell
  • Ships in: 2 business days
  • Transit time: Up to 5 business days
  • Delivery by: Jan 02 to Jan 04
  • Notes: Brand New Book. Order Now.

Code of Federal Regulations Title 21, Volume 1, April 1, 2016 contains regulations governing Food and Drugs and may also be referenced as:

- Code of Federal Regulations Title 21, Volume 1, April 1, 2016
- CFR Title 21
- CFR 21, Food and Drugs
- CFR 21, Parts 1 to 99, Food and Drugs

This volume contains Parts 1 to 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 RlC%

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