Showing results for IRB

Summit: Welcome to Clinical Research
By the end of this course, you should be able to: Describe how protocols direct the conduct of a study. Detail how informed consent is obtaine...
Biomed Refresher 3 – History and Ethical Principles – Research vs. Practice
Reviews the basic modules History and Ethics of Human Subjects Research and Basic Institutional Review Board (IRB) Regulations and Process. Distinguis...
Biomed Refresher 3 – History and Ethical Principles – Belmont Principles
Provides a review of the key themes from the basic modules History and Ethics of Human Subjects Research and Basic Institutional Review Board (IRB) Re...
Phase I Research: Protecting Phase I Subjects
Reviews U.S. Food and Drug Administration (FDA) requirements for initiation of phase I research studies following non-clinical studies. Describes IRB ...
On Tech Ethics Podcast - Citizen or Participatory Science Ethics
Season 1 - Episode 29 - Citizen or Participatory Science Ethics Discusses citizen or participatory science, including its benefits and key ethical is...
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