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Get the free Common Rule Consent Form Guidance - University of Alberta

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RESEARCH ETHICS OFFICE201 North Power Plant, 11312 89 Ave Edmonton, Alberta, Canada T6G 2N2 Tel: 780.492.0459 reoffice Alberta.ca uab.ca/reoUniversity of Alberta Research Ethics Board Policy on Signing
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How to fill out common rule consent form

01
Start by reading the common rule consent form thoroughly to understand what is being asked of you.
02
Provide your personal information such as your name, address, and contact details.
03
Understand the purpose of the study or research being conducted and the potential risks and benefits involved.
04
Make sure to ask any questions or seek clarification on any points you're unsure of.
05
Sign and date the consent form to indicate your agreement and understanding of the information provided.
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Keep a copy of the completed consent form for your records.

Who needs common rule consent form?

01
Common rule consent forms are needed by individuals participating in studies or research that are governed by the 'Common Rule'. This typically includes participants in medical or scientific research studies conducted by universities, medical institutions, government agencies, or private organizations.
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The Common Rule consent form is a standard document used in research involving human subjects that outlines the rights of participants, the nature of the research, and the voluntary nature of participation.
Researchers conducting studies that involve human subjects must file the Common Rule consent form to ensure compliance with federal regulations.
To fill out the Common Rule consent form, researchers should provide clear information about the study, including its purpose, procedures, risks, benefits, and contact information for questions, along with a signature line for participants.
The purpose of the Common Rule consent form is to inform participants about the research study, ensuring they understand their rights and can make an informed decision about their participation.
The Common Rule consent form must include details about the study's purpose, procedures, risks, benefits, confidentiality measures, voluntary participation, and contacts for inquiries.
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