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FACULTY OF HUMANITIES RESEARCH ETHICS COMMITTEE REVIEW TEMPLATE 2019.02.12 (V4)Name of Applicant Title of Project Degree Department Supervisor/s Date of REC meeting GENERAL ASPECTS YesNoCommentIs
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How to fill out templates for informed consent

01
Start by clearly outlining the purpose of the research or medical procedure in the template.
02
Provide detailed information about the risks and benefits involved, including any potential side effects or complications.
03
Clearly explain the participant's rights and responsibilities, as well as any confidentiality agreements.
04
Include a section for the participant to sign and date, indicating their informed consent.
05
Make sure to provide a copy of the completed template to the participant for their records.

Who needs templates for informed consent?

01
Researchers conducting experiments or studies involving human subjects.
02
Healthcare professionals obtaining consent for medical procedures or treatments.
03
Institutions or organizations conducting clinical trials or research studies.
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Informed consent templates provide a standardized format for explaining the research study to participants and ensuring they understand the risks and benefits before agreeing to participate.
Researchers and institutions conducting studies that involve human subjects are required to use templates for informed consent.
Templates for informed consent are typically filled out by researchers or study coordinators, following the guidelines provided by their institution or regulatory bodies.
The purpose of templates for informed consent is to protect the rights and well-being of research participants by ensuring they have all the necessary information to make an informed decision about participating in a study.
Templates for informed consent should include details about the study objectives, procedures, risks and benefits, confidentiality, voluntary participation, and contact information for questions or concerns.
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