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INFORMED CONSENT FORM We collect your personal information and use it to help us: give you services contact you keep your information safe on a computer and/or in a paper file. We may share your information
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01
Read through the entire informed consent form carefully.
02
Make sure to understand all the information provided in the form.
03
Fill in your personal details accurately and truthfully.
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Sign and date the form to indicate your agreement to participate.
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Keep a copy of the signed form for your records.

Who needs informed consent form we?

01
Individuals who are participating in a research study.
02
Patients who are undergoing a medical procedure or treatment.
03
Participants in a clinical trial.
04
Individuals receiving counseling services.
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Informed consent form is a document that explains the risks and benefits of a medical procedure, treatment, or research study to a patient or participant.
Healthcare professionals, researchers, or organizations conducting medical procedures, treatments, or research studies are required to file informed consent forms.
To fill out an informed consent form, one must carefully read the provided information, ask any questions for clarification, and then sign the form to indicate understanding and agreement.
The purpose of informed consent form is to ensure that individuals understand the risks and benefits of a medical procedure, treatment, or research study before agreeing to participate.
Informed consent form must include details about the procedure, treatment, or study, potential risks, benefits, alternatives, confidentiality, and contact information for questions or concerns.
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