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Informed Consent and Confidentiality Template International University for Graduate StudiesVisit the BUGS web page Policy on Research Ethics Involving Human Participants and Personal Data to download
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To fill out the IUGS informed consent form, follow these steps:
02
Start by reading the entire form carefully to understand its content and purpose.
03
Fill in the personal information section, providing your name, address, and contact details.
04
Make sure to thoroughly understand the risks and benefits of the proposed procedure or treatment mentioned in the form.
05
If you have any doubts or questions, seek clarification from the healthcare professional or researcher involved.
06
Date and sign the informed consent form, indicating your understanding of its contents and your agreement to participate.
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Keep a copy of the completed form for your records.
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Return the original signed form to the responsible party or healthcare organization.
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Note: It is essential to ensure that you have a comprehensive understanding of the information provided, as your consent is based on your informed decision.

Who needs iugs informed consent?

01
The IUGS informed consent is needed by individuals who are being asked to participate in a research study or undergo a medical procedure.
02
This includes patients, volunteers, or any person who may be directly involved in the study or treatment.
03
The purpose of the informed consent is to ensure that individuals have understood the potential risks, benefits, and purposes of their involvement and have given their voluntary and informed consent to participate.
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IUGS informed consent refers to the consent obtained from participants before conducting any research or study that involves them. It ensures that the participants are well-informed about the purpose, risks, and benefits of the study.
Researchers, scientists, or anyone conducting a study that involves human participants are required to obtain and file IUGS informed consent.
To fill out IUGS informed consent, researchers should provide detailed information about the study, its purpose, procedures, risks, benefits, and ensure that participants understand and agree to participate.
The purpose of IUGS informed consent is to protect the rights and well-being of participants in research studies by ensuring that they understand the study, its risks, benefits, and voluntarily agree to participate.
IUGS informed consent should include information about the study's purpose, procedures, risks, benefits, confidentiality, compensation (if any), and contact information for questions or concerns.
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