What information is included in the informed consent process?

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Information included in the informed consent process, at a minimum, includes:

  • What all exactly will be done/administered to the subject
  • The plan for the protocol and how it works
  • Any risks or discomforts they will be exposed to or may experience
  • A reminder that participation is completely voluntary, and they may leave at any point they decide

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This post was written by ClinicalTrialAdmin