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Sample Consent Form Western Carolina University Department of Human Services Killian 204 Callower, NC 28723 Phone: 8282277310 Fax: 8282277021Principal Investigator (PI): Eliza Dean, Ph.D. Phone: 8282273349
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How to fill out informed consent form

01
Read the informed consent form carefully to understand its purpose and what you are consenting to.
02
Provide your personal information, such as your name, address, and contact details.
03
Ensure you understand the risks, benefits, and alternatives associated with the procedure or study you are consenting to.
04
Ask any questions you may have and seek clarification from the person administering the consent form.
05
If you are satisfied with the information provided, sign and date the consent form.
06
Keep a copy of the signed consent form for your records.
07
If you have any concerns or changes in your condition, inform the relevant healthcare professional or researcher.

Who needs informed consent form?

01
Anyone participating in medical research studies or clinical trials.
02
Patients undergoing medical procedures, surgeries, or treatments.
03
Individuals seeking specialized treatments or alternative therapies.
04
People participating in psychological or social studies.
05
Minors or individuals who are unable to provide informed consent themselves may require a guardian or authorized representative to sign the form on their behalf.

What is Ined Consent - Western Carolina University Form?

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An informed consent form is a document that provides potential participants in a study or medical procedure with comprehensive information about the risks, benefits, and purpose of the study, ensuring that they understand and voluntarily agree to participate.
Researchers and institutions conducting studies involving human participants are required to file informed consent forms to comply with ethical and legal standards.
To fill out an informed consent form, you should carefully read the information provided, ensure you understand the details about the study, ask any questions you may have, and confirm your consent by signing and dating the document.
The purpose of the informed consent form is to protect the rights of participants by ensuring they are fully informed about the study and to document their agreement to participate.
The informed consent form must include information on the study's purpose, procedures, risks, benefits, confidentiality protections, and the right to withdraw at any time.
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