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Este documento presenta una guía para redactar un consentimiento informado específico para cualquier estudio que involucre sujetos humanos y que se presente a la SAU IRB para su revisión. Incluye los elementos básicos necesarios para el consentimiento informado y se debe escribir en un lenguaje accesible para los participantes del estudio.
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How to fill out informed consent form

How to fill out informed consent form
01
Begin by reading the entire informed consent form carefully.
02
Ensure that all sections are complete and clear, including the purpose of the study or procedure.
03
Review the risks and benefits outlined in the form.
04
Confirm that the privacy and confidentiality measures are clearly stated.
05
If applicable, check for information regarding compensation or costs involved.
06
Ask questions to the researcher or practitioner if any part is unclear or if you need further information.
07
Once you are satisfied with your understanding, complete any required personal information fields.
08
Sign and date the form to indicate your consent.
Who needs informed consent form?
01
Participants in clinical trials or research studies.
02
Patients undergoing medical procedures or treatments.
03
Subjects in psychological studies.
04
Individuals providing data for surveys or interviews.
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What is informed consent form?
An informed consent form is a document that outlines the details of a medical procedure or research study, ensuring that a participant is fully aware of what it entails, including risks, benefits, and alternatives before agreeing to partake.
Who is required to file informed consent form?
Researchers, healthcare providers, or organizations conducting clinical trials, studies, or interventions involving human subjects are required to file an informed consent form.
How to fill out informed consent form?
To fill out an informed consent form, read the document carefully, ensure all sections are completed, provide necessary personal information, and sign to indicate understanding and agreement.
What is the purpose of informed consent form?
The purpose of an informed consent form is to protect the rights of participants by ensuring they are aware of the details and implications of their involvement, promoting autonomy and informed decision-making.
What information must be reported on informed consent form?
The informed consent form must report information such as the purpose of the study, procedures involved, potential risks and benefits, confidentiality measures, and the participant's right to withdraw at any time.
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