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Standard Informed Consent Form THUS Version 2.0 September 2021 This document is meant as a standard text in which you as researcher inform the participants of your research about their cooperation

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How to fill out standard informed consent form

01

Begin by reading the entire informed consent form carefully to understand the purpose and details of the study or procedure.

02

Fill in your personal information such as your name, age, contact details, and any other requested details.

03

Make sure to review the risks and benefits section thoroughly and understand the potential consequences of participating.

04

If you have any concerns or questions, ask the researcher or physician before signing the form.

05

Sign and date the consent form to indicate your agreement to participate voluntarily.

06

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

Who needs standard informed consent form?

01

Anyone who is participating in a research study or medical procedure that requires informed consent.

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What is standard informed consent form?

A standard informed consent form is a document that provides potential participants with information about a study or procedure, allowing them to make an informed decision about their participation.

Who is required to file standard informed consent form?

Researchers and institutions conducting clinical trials or studies involving human participants are typically required to file a standard informed consent form.

How to fill out standard informed consent form?

To fill out a standard informed consent form, provide clear information about the study's purpose, procedures, risks, benefits, confidentiality, and the right to withdraw. Ensure that participants understand the information before they sign.

What is the purpose of standard informed consent form?

The purpose of a standard informed consent form is to protect the rights and welfare of participants by ensuring they are adequately informed about the study and consenting voluntarily.

What information must be reported on standard informed consent form?

The form must report details such as the study's purpose, duration, procedures, potential risks, benefits, confidentiality measures, and the right to withdraw at any time.

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