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Participate in a study assessing the effectiveness of daily and weekly iron supplementation in preventing anemia in infants and its impact on genomic stability.
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Make sure you read and understand the information provided in the informed consent form
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Who needs informed consent form?

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Informed consent form is typically required for medical procedures, clinical trials, research studies, and other situations where an individual's participation or consent is needed
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An informed consent form is a document that outlines the risks, benefits, and alternatives to a medical procedure or research study, and is signed by the participant or patient to indicate their understanding and agreement.
Researchers, medical professionals, or any individuals conducting a study or medical procedure involving human participants are required to file an informed consent form.
The informed consent form should be filled out by providing clear and detailed information about the procedure or study, including risks, benefits, and alternatives. Participants should be given the opportunity to ask questions and have a full understanding before signing the form.
The purpose of an informed consent form is to ensure that participants are fully informed about the risks and benefits of a medical procedure or research study, and voluntarily agree to participate.
The informed consent form must include information on the nature of the study or procedure, potential risks and benefits, confidentiality measures, and contact information for questions or concerns.
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