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IRB Approved Template MUST BE APPROVED FOR SITES BEFORE USE AS MODIFIED Jan 22, 2021MAIN INFORMED CONSENT FORM (ICF) AND PARENTAL PERMISSION FORM FOR AGES 12 17 YEARS OLD TITLE:A Phase 3, Randomized,
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To fill out the main informed consent form, follow these steps:
02
Begin by reading the form thoroughly to understand its contents.
03
Provide your personal information such as name, address, phone number, and email address in the designated fields.
04
Carefully review the purpose, procedures, and risks associated with the study or treatment being conducted.
05
Make sure you understand the voluntary nature of participation and your right to withdraw at any time.
06
If you have any questions or concerns, contact the researcher or medical professional responsible for the study.
07
Sign and date the form to indicate your informed consent to participate.
08
Keep a copy of the filled-out form for your records.
09
Submit the form to the appropriate authority or research institution.
10
It is advisable to obtain a copy of the signed form for your reference.

Who needs main informed consent form?

01
The main informed consent form is typically needed by individuals who are participating in a research study, clinical trial, or medical treatment. It is crucial for ensuring that participants are fully informed about the purpose, procedures, potential risks, and benefits associated with the study or treatment. This form helps protect the rights and well-being of the participants by obtaining their voluntary consent to participate based on comprehensive information.
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The main informed consent form is a document that outlines the details of a research study and allows participants to understand and voluntarily agree to participate.
Researchers or institutions conducting a research study are required to file the main informed consent form.
The main informed consent form is typically filled out by providing information about the study, risks and benefits, confidentiality, and a space for participants to sign and date.
The purpose of the main informed consent form is to ensure that participants are fully informed about the study they are part of and willingly agree to participate.
The main informed consent form must include details about the study objectives, procedures, risks and benefits, confidentiality, participant rights, and contact information for questions or concerns.
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