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Informed consent is a crucial element of clinical trials, with ethical and regulatory implications highlighted in the previous module. This module will focus on the specifics of the informed consent process and detail nine key components that constitute any informed consent document. Learning objectives include understanding the informed consent process basics, identifying the nine elements, and applying them to research study documents. Informed consent is a standardized process ensuring participants receive all necessary information to make an informed, voluntary decision, and it must be comprehensible and free of exculpatory clauses. Afterward, there will be a knowledge check to assess understanding.