Informed consent form (ICF) must not only satisfy local and international regulatory requirements but represent a communication between potential research participant and the clinical personnel about the main aspects of clinical trial and participant’s involvement in it. ICF is a critical to participant’s willingness to enroll or continue in the clinical study.

The job of a MW is to clearly describe clinical, personal and legal information to the potential participant in an objective and ethical manner making sure that participants are confident about their own understanding of the conduct, potential benefits and risks of the trial.