Institutional Review Board (IRB)

An Institutional Review Board (IRB) is a critical committee responsible for safeguarding the rights and welfare of human subjects in research studies. Coursera's Institutional Review Board (IRB) catalogue teaches you the fundamental principles of research ethics, regulatory requirements, and the IRB review process. You'll learn to evaluate research protocols, assess risks and benefits, ensure informed consent, protect vulnerable populations, and apply ethical guidelines in various research contexts. Mastering IRB processes empowers you to contribute to ethical research practices, enhance participant protection, and maintain the integrity of scientific studies across academic, medical, and professional settings.
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Results for "institutional review board (irb)"

  • Status: Free Trial

    Novartis

    Skills you'll gain: Good Clinical Practices (GCP), Informed Consent, Clinical Research, Clinical Trials, Clinical Research Ethics, Institutional Review Board (IRB), Drug Development, Record Keeping, Clinical Documentation, Regulatory Compliance, Patient Communication

    4.8
    Rating, 4.8 out of 5 stars
    196 reviews

    Beginner · Course · 1 - 4 Weeks

  • Status: Preview

    Fred Hutchinson Cancer Center

    Skills you'll gain: Data Ethics, Data Sharing, Personally Identifiable Information, Clinical Research Ethics, Institutional Review Board (IRB), Healthcare Ethics, Data Security, Data Governance, Information Privacy, Health Insurance Portability And Accountability Act (HIPAA) Compliance, Health Information Management, Informed Consent, Encryption

    Beginner · Course · 1 - 4 Weeks

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  • Johns Hopkins University
  • Novartis
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  • University of Michigan
  • Fred Hutchinson Cancer Center
  • Universidad Nacional Autónoma de México