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Patient Information Leaflet/Consent Form Template for Biomarker/Biobanking studies Guidance for using this template document: ? Use simple, clear language: o Font size should not be less than size
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Patient information leaflet/consent form is a document that provides detailed information about a medical treatment, procedure, or clinical trial to patients or participants, including benefits, risks, and possible outcomes, as well as obtaining their consent.
Healthcare providers, researchers, or organizations conducting medical treatments, procedures, or clinical trials are required to provide and file patient information leaflet/consent form.
The patient information leaflet/consent form is typically filled out by healthcare providers or researchers, ensuring all necessary information is disclosed to the patient or participant, and obtaining their signature indicating consent.
The purpose of patient information leaflet/consent form is to inform patients or participants about the treatment, procedure, or trial being performed, the risks and benefits involved, and to obtain their voluntary consent to proceed.
Patient information leaflet/consent form must include details about the treatment, procedure, or trial, potential risks and benefits, alternatives, confidentiality, contact information, and signature lines for the patient or participant.
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