What Is Obtain Consent

Obtaining consent involves explaining the research and assessing participant comprehension using a consent document, usually a written consent form or information sheet, as a guide for the verbal explanation of the study.

What is obtaining informed consent?

Summary. When conducting clinical research, the obtaining of informed consent is required. Informed consent is a procedure through which a competent subject, after having received and understood all the research-related information, can voluntarily provide his or her willingness to participate in a clinical trial.

When should consent be obtained?

Written consent should always be taken where: There are significant risks or side effects associated with the proposed treatment or procedure. The patient’s lifestyle, employment or personal relationships could be adversely affected by the outcome of the treatment or procedure.

Marcus Vance

Marcus Vance

Cybersecurity & Digital Privacy Researcher

Marcus Vance is a cybersecurity auditor and technology writer dedicated to educating the public about online safety, data privacy regulations, enterprise security, and emerging cyber threats.

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