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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