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ACRP CCRC
ACRP CCRC
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Study Design, Adverse Event Classification, Documentation, & Reporting, Misc ...10Decks151Flashcards1,481Learners -
SOCRA 2023
SOCRA 2023
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21 CFR Part 11, 21 CFR Part 50, 21 CFR Part 56 ...16Decks488Flashcards444Learners -
SOCRA 2020
SOCRA 2020
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21 CFR Part 11, 21 CFR Part 50, 21 CFR Part 56 ...12Decks247Flashcards1,053Learners -
CCRP Prep
CCRP Prep
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Declaration of Helsinki, US Code of Federal Regulations2Decks57Flashcards2Learners -
SOCRA 2023
SOCRA 2023
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Nuremberg Code, Declaration of Helsinki, Belmont Report ...12Decks233Flashcards91Learners -
SOCRA CCRP Exam
SOCRA CCRP Exam
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21 CFR Part 11, 21 CFR Part 50, 21 CFR Part 56 ...12Decks187Flashcards175Learners -
SOCRA CCRP 2020
SOCRA CCRP 2020
By: Madison R
21 CFR Part 11, 21 CFR Part 50, 21 CFR Part 56 ...23Decks350Flashcards505Learners -
SOCRA_2015
SOCRA_2015
By: allison iwan
21 CFR Part 11, 21 CFR Part 50, 21 CFR Part 56 ...15Decks758Flashcards203Learners -
ACRP CPI®
ACRP CPI®
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ICH E2A Safety Monitoring, ICH E6R1 Good Clinical Practice, ICH E8 Clinical Development ...7Decks600Flashcards10Learners -
ACRP - MDP Subspeciality
ACRP - MDP Subspeciality
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Declaration Of Helsinki (DOH), Abbreviation List, ICH-E2A ...13Decks724Flashcards5Learners -
SOCRA 2024
SOCRA 2024
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FDA Forms, Ethical guidelines and Regulations, Declaration of Helsinki ...9Decks244Flashcards13Learners -
ACRP - CCRC Exam
ACRP - CCRC Exam
By: Patrick Campbell
Declaration of Helsinki, ICH Abbreviations - and definitions, ICH E2A Definitions and Standards for Expedited Reporting ...14Decks785Flashcards22Learners -
SOCRA CCRP EXAM
SOCRA CCRP EXAM
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45 CRF 46, 21 CFR 11, 21 CFR 50 ...17Decks337Flashcards38Learners -
acrp
acrp
By: Victor Obinna Durueke
AE classification, reporting, documentation, Study design, IRB ...7Decks120Flashcards13Learners -
HSPH
HSPH
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The Epidemiological Approach, Interpreting Data, Randomised Controlled Trials ...29Decks951Flashcards11Learners -
HSPH
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CAL 1, CAL 2, The Epidemiological Approach ...26Decks825Flashcards6Learners -
CCRP test
CCRP test
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CCRP virtual course, 21 code of federal regulations, Investigational New Drug Application ...15Decks412Flashcards43Learners -
ACRP Certification
ACRP Certification
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ICH E6 – Guideline for Good Clinical Practice/GCP, ICH E2 Clinical Safety Data Management, ICH E8- General Considerations for Studies ...11Decks505Flashcards3Learners -
SOCRA 2024 Flashcards
SOCRA 2024 Flashcards
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1 CRF Part 312 – Investigational New Drug Application, 21CFR50 – §50.20 Scope , 21 CFR 812– Investigational Device Exemption ...8Decks168Flashcards1Learner -
CCRC
CCRC
By: Ashley O’Neil
Clinical Safety Data Management, General Considerations for Clinical Trials, Statistical Principles in Clinical Trials ...22Decks326Flashcards3Learners