US FDA Code of Federal Regulations
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Last updated 4:55 AM on 2/17/25
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5 Terms
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21 CFR Part 11
Electronic records and signatures
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21 CFR Part 50
Protection of human subjects
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21 CFR Part 312
Investigational new drug application
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21 CFR Part 56
Institutional Review Boards (IRBs)
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Flashcards (57)