Informed Consent

The informed consent document and process are designed to serve as an ethical framework for safeguarding the rights and well-being of research participants. This course explains informed consent regulations and guidelines, the informed consent process, and the roles and responsibilities of clinical research professionals. Topics in this course include: Foundational Documents, Consent Document, Types, Exceptions, Pediatric Research, Managing Consent, and Verifying. After completing this course, learners will be able to identify key historical events that led to the current informed consent regulations and guidelines and will also be able to recognize the informed consent process as well as its documentation requirements.

After this course learners will be able to identify key historical events that led to the current informed consent regulations and guidelines. recognize the informed consent process as well as its documentation requirements.