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SHAHEED MONTANA BEHAVIOR BHUTTO INSTITUTE OF TRAUMA Department of Research & Development SAMPLE INFORMED CONSENT FORM This is a generic sample form to help you address most situations. Please adapt
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How to fill out informed consent form for

01
Read through the informed consent form thoroughly to understand all the details and requirements.
02
Fill in your personal information correctly and completely, such as your full name, address, contact details, and date of birth.
03
Review the sections related to the study or procedure being conducted and make sure you understand the purpose, risks, benefits, and alternatives.
04
Sign and date the form to indicate your agreement and consent to participate or undergo the procedure.
05
Keep a copy of the completed informed consent form for your records.

Who needs informed consent form for?

01
Informed consent forms are required for individuals participating in research studies, clinical trials, medical procedures, surgeries, and other activities where consent is needed for legal and ethical reasons.
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The informed consent form is used to document the voluntary agreement of an individual to participate in a research study or medical treatment.
Researchers, medical professionals, and anyone conducting a study or procedure that requires informed consent are required to file informed consent forms.
The informed consent form should be filled out by providing detailed information about the study or treatment, risks and benefits, confidentiality, and the participant's rights.
The purpose of the informed consent form is to ensure that individuals understand the nature of the study or treatment, and voluntarily agree to participate.
The informed consent form must include details about the study or treatment, risks and benefits, confidentiality, participant's rights, and contact information for questions or concerns.
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