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INFORMED CONSENT FOR A STUDY PRIOR TO PREIMPLANTATION GENETIC TESTING FOR MONOTONIC DISEASES (PREP GTM) DESCRIPTION, PURPOSE AND ADVANTAGES OF PERFORMING THE ANALYSIS PreP GTM entails conducting a
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Anyone who is considering participating in a study or procedure that requires informed consent should fill out an informed consent form. This includes individuals who are of legal age to provide consent and have the mental capacity to understand the information provided.
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Informed consent is a process whereby individuals are informed about the risks, benefits, and alternatives of a particular procedure or treatment, allowing them to make an educated decision about whether to proceed.
Typically, healthcare providers, researchers, and institutions conducting studies or treatments involving human participants are required to obtain and file informed consent.
To fill out informed consent, provide clear information about the procedure, its purpose, potential risks and benefits, alternatives, and ensure that the participant understands and voluntarily agrees by signing the document.
The purpose of informed consent is to protect the autonomy and rights of individuals by ensuring they are adequately informed before participating in treatments or research.
Informed consent should include the purpose of the study or treatment, description of the procedures involved, potential risks and benefits, alternatives to participation, and confidentiality assurances.
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