Informed Consent Form Template

If you are performing a clinical research study, this Informed Consent Form template will allow you to collect your participants’ consent in minutes. Our form builder records each person’s yes or no, and then you can utilize those responses to determine how to use each person’s data in the clinical trial.

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Frequently Asked Questions

Informed consent is a principle in medical treatment and research where the medical staff is obligated to give the patient sufficient information about the treatment’s consequences. An informed consent form is a document that outlines this information and that the patient has to sign to agree. The practice of using consent forms regarding medical studies and clinical trials is common in many countries.

You can customize our consent form template using our form builder. Firstly, duplicate the template in your 123FormBuilder account. Then, edit the form with your knowledgeable consent version and other features you see fit. 123FormBuilder makes it easy to create online forms using a user-friendly designer with drag-and-drop functionality.

The purpose of this form is to inform your potential participants what you plan to ask them to do during your study so that they can decide if they want to participate. You should detail the following areas: participation time requirement, participant tasks, communication, risks, compensation, confidentiality, freedom to withdraw, dissemination of results, and contact information for the Principal Investigator.

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