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[Other logos may be entered e.g., Research Center]INFORMED CONSENT (For studies where there is no processing of personal data of the participants)This study is part of a research project taking place

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How to fill out informed consent

01

Provide a clear explanation of the study or procedure and its risks and benefits.

02

Ensure the participant understands the information provided.

03

Allow the participant time to ask questions and clarify any concerns.

04

Obtain written consent from the participant or their legal guardian.

05

Provide a copy of the signed informed consent form to the participant for their records.

Who needs informed consent?

01

Informed consent is typically required for any study or medical procedure involving human subjects, including clinical trials, research studies, and medical interventions.

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What is informed consent?

Informed consent is a process for getting permission before conducting a healthcare intervention on a person.

Who is required to file informed consent?

Informed consent is typically required to be filed by healthcare providers such as doctors, nurses, and other medical professionals.

How to fill out informed consent?

Informed consent is usually filled out by the healthcare provider and signed by both the provider and the patient or their legal guardian.

What is the purpose of informed consent?

The purpose of informed consent is to ensure that patients understand the risks, benefits, and alternatives to a medical intervention before agreeing to it.

What information must be reported on informed consent?

Informed consent forms usually include information about the specific procedure, risks involved, expected outcomes, and alternative treatment options.

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