Title 21 Code of Federal Regulations (CFR): Food and Drugs
21 CFR PART 11—ELECTRONIC RECORDS; ELECTRONIC SIGNATURES
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21 CFR PART 50—PROTECTION OF HUMAN SUBJECTS
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21 PART 54—FINANCIAL DISCLOSURE BY CLINICAL INVESTIGATORS
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21 PART 56—INSTITUTIONAL REVIEW BOARDS
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21 PART 58—GOOD LABORATORY PRACTICE FOR NONCLINICAL LABORATORY STUDIES
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21 CFR 211 – CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS
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PART 312—INVESTIGATIONAL NEW DRUG APPLICATION
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21 CFR 314 – APPLICATIONS FOR FDA APPROVAL TO MARKET A NEW DRUG
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PART 812—INVESTIGATIONAL DEVICE EXEMPTIONS
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PART 814—PREMARKET APPROVAL OF MEDICAL DEVICES
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PARTS 600 to 799 FOR BIOLOGICS AND COSMETICS
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