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Institutional Review Board Informed Consent Document for Research Principal Investigator: Study Title: Institution/Hospital:Revision Date:This informed consent document applies to (Example: adults,

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How to fill out this informed consent document

01

Read the informed consent document thoroughly and carefully before filling it out.

02

Start by providing personal information such as your name, address, and contact details.

03

Understand the purpose and nature of the activities or procedures for which consent is being sought.

04

Make sure you comprehend the risks, benefits, and potential alternatives involved.

05

If you have any questions or concerns, don't hesitate to seek clarification from the relevant parties.

06

Consider seeking legal or professional advice if needed.

07

Once you are satisfied and have a clear understanding, sign and date the informed consent document.

08

Keep a copy of the signed document for your records.

Who needs this informed consent document?

01

Any individual who is participating in a research study, clinical trial, medical procedure, or any activity that requires their informed consent.

02

Healthcare professionals and researchers who are conducting studies, experiments, or trials involving human subjects.

03

Legal entities, institutions, or organizations that are responsible for ensuring informed consent is obtained from individuals.

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What is this informed consent document?

This informed consent document is a legal form that outlines the risks and benefits of participating in a research study or medical procedure.

Who is required to file this informed consent document?

The individuals participating in the research study or medical procedure are required to sign and file this informed consent document.

How to fill out this informed consent document?

The informed consent document should be read thoroughly, signed voluntarily, and any questions should be clarified with the researcher or healthcare provider before signing.

What is the purpose of this informed consent document?

The purpose of this informed consent document is to ensure that individuals understand the risks, benefits, and procedures involved in a research study or medical procedure before making a decision to participate.

What information must be reported on this informed consent document?

The informed consent document must include details about the study or procedure, potential risks and benefits, confidentiality, voluntary participation, and contact information for questions and concerns.

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