Overview
This comprehensive module provides the key concepts of informed consent. It explains the components of a complete and appropriate consent form as specified by the International Conference on Harmonisation (ICH) and the US Food and Drug Administration (FDA), as well as guidance for the creation and appropriate wording of these components. It also includes a discussion on the benefits and concerns with electronic informed consent, and presents publications and projects that explore the use of eConsent.
The module takes an average of 4 hours to complete.
This eLearning module can be purchased individually or as part of the Clinical Trial Management Comprehensive eLearning Bundle.
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