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Mod. PR 11. L15 ENG rev.04-Page 1 of 4INFORMED CONSENT FOR THE PROCESSING OF GENETIC ANALYSIS (Minors and people with legal guardians) The undersigned Date of birthplace of birth Resident of Province
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Anyone who is participating in a research study, clinical trial, medical procedure, or any activity that involves potential risks and requires the individual's informed consent.
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Informed consent for form is a legal document that ensures that a participant is fully informed about the procedures, risks, benefits, and purpose of a study or treatment before agreeing to participate.
Researchers, healthcare providers, and institutions conducting biomedical or behavioral studies are required to file informed consent forms.
To fill out an informed consent form, provide clear information about the study, including its purpose, procedures, risks, benefits, and confidentiality, and then obtain the participant's signature to indicate their consent.
The purpose of the informed consent form is to protect the rights and welfare of participants by ensuring they understand what participation involves before they agree to it.
The informed consent form must report the study's purpose, procedures, potential risks, benefits, confidentiality measures, and the right to withdraw from the study at any time.
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