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

    University of Michigan

    Skills you'll gain: Institutional Review Board (IRB), Clinical Trials, Clinical Research, Clinical Research Ethics, Healthcare Ethics, Good Clinical Practices (GCP), Medical Science and Research, Drug Development, Research, Health Policy, Pharmaceuticals, Patient Safety

  • 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