Get the free Research Consent and Authorization Form - ClinicalTrials.gov

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CONSENT FORM PARTICIPANT THIS FORM WILL BE HELD FOR A PERIOD OF 6 Paramedical and Health Sciences 85 Park Road, Grafton pH: (09) 923 2760 www.fmhs@auckland.ac.nz The University of Auckland Private

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How to fill out research consent and authorization

01

Read the research consent form thoroughly to understand the purpose of the study, procedures involved, risks and benefits, and your rights as a participant.

02

Sign and date the consent form to indicate your willingness to participate in the research study.

03

Make sure to ask any questions you may have before signing the consent form.

04

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

Who needs research consent and authorization?

01

Anyone who is being asked to participate in a research study as a subject or participant needs research consent and authorization.

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What is research consent and authorization?

Research consent and authorization are processes by which individuals voluntarily agree to participate in a research study and provide permission for researchers to collect and use their personal data.

Who is required to file research consent and authorization?

Researchers conducting studies that involve human subjects are required to obtain and file research consent and authorization.

How to fill out research consent and authorization?

Research consent and authorization forms are typically filled out by participants themselves or by their legal guardians if they are minors. The forms should include information about the study, risks and benefits, confidentiality, and how to withdraw consent.

What is the purpose of research consent and authorization?

The purpose of research consent and authorization is to ensure that participants are fully informed about the study, its risks and benefits, and to enable them to make a voluntary decision to participate.

What information must be reported on research consent and authorization?

Research consent and authorization forms must include details about the study, risks and benefits, confidentiality measures, contact information for the researcher, and information on how to withdraw consent.

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