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CFR 21, Parts 1 to 99, Food and Drugs, April 01, 2016 (Volume 1 of 9)
CFR 21, Parts 1 to 99, Food and Drugs, April 01, 2016 (Volume 1 of 9)
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130,29 €
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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 DrugsThis 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; ORGAN…
  • Publisher:
  • ISBN-10: 1359980180
  • ISBN-13: 9781359980182
  • Format: 15.6 x 23.4 x 2.9 cm, softcover
  • Language: English
  • SAVE -10% with code: EXTRA

CFR 21, Parts 1 to 99, Food and Drugs, April 01, 2016 (Volume 1 of 9) (e-book) (used book) | bookbook.eu

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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 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

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  • Publisher:
  • ISBN-10: 1359980180
  • ISBN-13: 9781359980182
  • Format: 15.6 x 23.4 x 2.9 cm, softcover
  • Language: English English

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 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

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