Learn Ich E6
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ACRP CCRA - ICH
ACRP CCRA - ICH
By: Jane Hand
Guideline for Good Clinical Practice E6(R2), Definitions and Standards for Expedited Reporting E2A, General Considerations for Clinical Trials E8 (R1) ...6Decks804Flashcards2Learners -
ACRP CCRA
ACRP CCRA
By: amy nguyen
Study Design, Adverse Event Classification, Documentation, & Reporting, Certification Exam Prep ...13Decks460Flashcards308Learners -
ACRP - CCRC Exam
ACRP - CCRC Exam
By: Patrick Campbell
Declaration of Helsinki, ICH Abbreviations - and definitions, ICH E2A Definitions and Standards for Expedited Reporting ...14Decks785Flashcards110Learners -
ACRP - MDP Subspeciality
ACRP - MDP Subspeciality
By: Courtney Elliott
Declaration Of Helsinki (DOH), Abbreviation List, ICH-E2A ...13Decks724Flashcards13Learners -
SOCRA 2023
SOCRA 2023
By: Eric Nguyen
21 CFR Part 11, 21 CFR Part 50, 21 CFR Part 56 ...16Decks488Flashcards909Learners -
ORTHO SOCRA PREP
ORTHO SOCRA PREP
By: Rebecca Smith
Glossary ICH E6(R2), ICH Harmonised Tripartite Guideline E2A, ICH E6(R2) ...10Decks225Flashcards18Learners -
SOCRA CCRP Exam
SOCRA CCRP Exam
By: Kaitlin K
21 CFR Part 11, 21 CFR Part 50, 21 CFR Part 56 ...12Decks187Flashcards254Learners -
ACRP Certification
ACRP Certification
By: Kassandra Nealon
ICH E6 – Guideline for Good Clinical Practice/GCP, ICH E2 Clinical Safety Data Management, ICH E8- General Considerations for Studies ...11Decks505Flashcards39Learners -
Socra Study
Socra Study
By: Shay Lavon Robison
Ethics Codes, Vocab, ICH GCP ...14Decks420Flashcards75Learners -
Socra
Socra
By: Jessica Torres
Session 1, Session 2, Session 3 ...11Decks563Flashcards57Learners -
SOCRA 2024
SOCRA 2024
By: Erin Clements
Nuremburg, Helsinki, Belmont, 45 CFR Part 46, 21 CFR Part 312 ...11Decks421Flashcards142Learners -
ccrp exam
ccrp exam
By: Victoria Williams
Title 21, Part 56 - IRB, Title 21, Part 312 - Investigational New Drug Application (IND), Title 21, Part 50 - Protection of Human Subjects ...14Decks160Flashcards1Learner -
SOCRA CCRP EXAM
SOCRA CCRP EXAM
By: Dylan drum
45 CRF 46, 21 CFR 11, 21 CFR 50 ...17Decks337Flashcards74Learners -
CCRP test
CCRP test
By: Erin Larsen
CCRP virtual course, 21 code of federal regulations, Investigational New Drug Application ...15Decks412Flashcards62Learners -
IRB AI Class
IRB AI Class
By: Andy Parkhurst
Historical Background, Research Ethics, Belmont Report ...21Decks538Flashcards1Learner -
CCRP
CCRP
By: Oliver Chiu
Investigator roles/responsibilities, Sponsor's roles/responsibilities, Reporting Timelines ...10Decks214Flashcards8Learners -
US Medical Device Regulations
US Medical Device Regulations
By: Suzanne Wertz
US Glossary, US History (Ch. 1), Overview of US Regulatory Pathways (Ch. 2) ...11Decks1,132Flashcards8Learners -
CCRP
CCRP
By: Dylan Drum
The CITI Good Clinical Practice Course for Clinical Trials with Investigational Drugs and Medical Devices, Overview of New Drug Development, Overview of ICH GCP ...13Decks86Flashcards27Learners -
SOCRA CCRP Exam Content
SOCRA CCRP Exam Content
By: Somia Sadruddin
The Nuremberg Code (1947), The Belmont Report (1979), The Declaration of Helsinki (1964) ...9Decks89Flashcards2Learners