21 C.F.R. CHAPTER I--FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
TITLE 21--Food and Drugs
CHAPTER I--FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
SUBCHAPTER A--GENERAL
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| GENERAL ENFORCEMENT REGULATIONS
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| GENERAL ADMINISTRATIVE RULINGS AND DECISIONS
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| ADMINISTRATIVE PRACTICES AND PROCEDURES
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| ELECTRONIC RECORDS; ELECTRONIC SIGNATURES
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| FORMAL EVIDENTIARY PUBLIC HEARING
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| PUBLIC HEARING BEFORE A PUBLIC BOARD OF INQUIRY
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| PUBLIC HEARING BEFORE A PUBLIC ADVISORY COMMITTEE
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| PUBLIC HEARING BEFORE THE COMMISSIONER
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| REGULATORY HEARING BEFORE THE FOOD AND DRUG ADMINISTRATION
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| CIVIL MONEY PENALTIES HEARINGS
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| STANDARDS OF CONDUCT AND CONFLICTS OF INTEREST
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| ENVIRONMENTAL IMPACT CONSIDERATIONS
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| 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
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| PROTECTION OF HUMAN SUBJECTS
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| FINANCIAL DISCLOSURE BY CLINICAL INVESTIGATORS
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| INSTITUTIONAL REVIEW BOARDS
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| GOOD LABORATORY PRACTICE FOR NONCLINICAL LABORATORY STUDIES
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| LISTING OF COLOR ADDITIVES EXEMPT FROM CERTIFICATION
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| LISTING OF COLOR ADDITIVES SUBJECT TO CERTIFICATION
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| COLOR ADDITIVE CERTIFICATION
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| GENERAL SPECIFICATIONS AND GENERAL RESTRICTIONS FOR PROVISIONAL COLOR ADDITIVES FOR USE IN FOODS, DRUGS, AND COSMETICS
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| LISTING OF CERTIFIED PROVISIONALLY LISTED COLORS AND SPECIFICATIONS
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| DISSEMINATION OF INFORMATION ON UNAPPROVED/NEW USES FOR MARKETED DRUGS, BIOLOGICS, AND DEVICES
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