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Patient consent form

A patient consent form is a legal contract between the patient and healthcare provider. It helps formalize the relationship between the parties involved, provides assurance of informed consent about medical treatment, and protects both parties in case of litigation relating to medical treatment. This document should be signed by the patient, allowing the clinician to provide services, but it does not obligate them to do so. The signature may take place electronically (for example via a digital tablet) or this may be done in writing on paper.

Time to complete

2 minutes

Eligibility

If you are 18 years of age or above, you are eligible to fill the Patient consent form.

Questions for Patient consent form

Name of the patient

The answer should be a text input.

Name of the Guardian

(If patient not signing this form)

The answer should be a text input.

Relationship to patient

(If patient not signing this form)

The answer should be a single choice:

Father
Mother
Sibling
Child
Friend
Other

I give my consent for the Material aboutme/the patient

The answer should be a single choice:

Agree
Disagree

I confirm that I

The answer should be a multiple choice:

have seen the photo, image, text or other material about me/the patient
have read the report to be submitted
am legally entitled to give this consent

Signature of the patient

The answer should be a signature.

Signature of the guardian

(If patient not signing this form)

The answer should be a signature.

Similar Ideas

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Patient Consent Form for Research Studies

Here are some FAQs and additional information
on Patient consent form

What is the Patient Consent form?

A document with important information about a medical procedure or treatment, a clinical trial, or genetic testing. It also includes information on possible risks and benefits. If a person chooses to take part in the treatment, or testing, he or she signs the form to give official consent.

Why is the Consent form important?

When barring a physical examination, informed consent is necessary for every medical examination and surgical procedure, which should be obtained in or in the presence of a disinterested party. Further, if any extension of the procedure is required which is not covered, fresh consent should be insisted.

What is Informed Consent?

As new medical products are being developed, no one knows for sure how well they will work, or what risks they will find. Clinical trials are used to answer questions such as, whether the new product is safe? how should the product be used? etc.

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