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Retain and analyze already collected data relating to the subject up to the time of subject's withdrawal; or. honor a research subject's request that the investigator destroy the subject's data or that the investigator exclude the subject's data from any analysis.
Withdrawal of consent was defined as a patient's voluntary termination of informed consent to participate in a clinical trial at any point during the conduct of the study.
In certain circumstances, a student may be withdrawn from study. This most commonly happens when a student has not met the deadline for submission of their thesis. It can also occur if a student is not progressing in their studies or has not paid their fees.
If a participant withdraws from a study either verbally or in writing, the participant's information, including PHI, should no longer be collected. This should be clearly outlined in the informed consent document.
Withdrawal of Consent is a legal term that refers to the process by which a person withdraws their consent to the terms of a contract. The act of withdrawing consent allows you to break your agreement with another party and avoid any penalties associated with non-compliance.