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Este formulario de consentimiento informará sobre un estudio de investigación diseñado para obtener comentarios sobre una nueva aplicación móvil destinada a ayudar a las personas a prepararse

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How to fill out informed consent form

01

Read the informed consent form thoroughly.

02

Identify the purpose of the study or procedure.

03

Review the risks and benefits outlined in the form.

04

Fill in your personal information, such as name and contact details.

05

Check the box or sign to indicate your voluntary agreement.

06

Ask questions if any part is unclear before signing.

07

Keep a copy of the signed consent form for your records.

Who needs informed consent form?

01

Participants in research studies.

02

Patients undergoing medical procedures or treatments.

03

Individuals participating in clinical trials.

04

Subjects in psychological, social, or behavioral studies.

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What is informed consent form?

An informed consent form is a document that explains the details of a medical procedure or research study to a participant, ensuring they understand the risks, benefits, and alternatives before agreeing to participate.

Who is required to file informed consent form?

Researchers, medical professionals, and organizations conducting experiments or medical treatments that involve human participants are required to file an informed consent form.

How to fill out informed consent form?

To fill out an informed consent form, one must read the entire document carefully, provide necessary personal information, acknowledge the understanding of the procedure, risks, and benefits, and sign and date the form.

What is the purpose of informed consent form?

The purpose of an informed consent form is to ensure that participants are fully aware of what they are agreeing to, to protect their rights, and to promote ethical standards in medical and research practices.

What information must be reported on informed consent form?

An informed consent form must report information such as the purpose of the study, procedures involved, potential risks and benefits, confidentiality assurances, and the right to withdraw consent at any time.

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