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CCRP
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informed consent Flashcards
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CCRP
(24 decks)
conflicts of interest
21 CRF Part 11
21 CFR Part 50
21 CFR part 56
21 CFR part 312
FDA forms
Belmont report
Nuremberg code
Misc. 2
ICF Harmonised Guideline for GCP
ICH clinical safety data management
investigator roles and responsibilities
sponsor's roles and responsibilities
IND reporting
informed consent
IRBs
Trial protocol and IB
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Additional
21 CFR part 812
45 CFR part 46
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