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UNIL I University de LausanneInformation Consent Form for Participants in Research Studies Please complete this form after you have read the Information Sheet and received an explanation about the

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How to fill out informed consent form for

01

Gather all the necessary information and documents related to the study or procedure for which the informed consent form is being filled out.

02

Read the informed consent form carefully to understand its content.

03

Provide detailed explanations and answer any questions or concerns the participant may have about the study or procedure.

04

Ensure that the participant has understood the information provided and is willing to participate voluntarily.

05

Have the participant sign and date the informed consent form to indicate their agreement to participate.

06

Make a copy of the signed informed consent form for both the participant and the researcher's records.

Who needs informed consent form for?

01

Anyone who is participating in a research study or medical procedure that involves potential risks, benefits, or implications needs an informed consent form.

02

This includes volunteers in clinical trials, patients undergoing experimental treatments, research participants, and individuals giving consent on behalf of minors or incapacitated persons.

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