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INFORMED CONSENT FOR PREIMPLANTATION GENETIC TESTING FOR MONOTONIC DISEASES (GTM) DESCRIPTION, PURPOSE AND ADVANTAGES OF PERFORMING THE ANALYSIS Preimplantation Genetic Testing for Monotonic Diseases
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Read the informed consent form carefully to understand the purpose, risks, benefits, and alternatives of the research or medical procedure.
02
Ensure that you have all the necessary information and have clarified any doubts or questions with the researcher or healthcare provider.
03
Provide your personal information such as name, age, contact details, and any relevant medical history as required.
04
Sign and date the informed consent form to indicate your willingness to participate or undergo the specific procedure.
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If applicable, ensure that a witness also signs the form to acknowledge your consent.
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Retain a copy of the signed informed consent form for your records.
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If you have any concerns or change your mind after providing consent, communicate with the researcher or healthcare provider as soon as possible.

Who needs informed consent for?

01
Informed consent is typically required for individuals who are participating in any research study or clinical trial.
02
It is also necessary for patients undergoing medical procedures, surgeries, or treatments that involve potential risks or experimental approaches.
03
Informed consent ensures that individuals are fully aware of the nature of the study or procedure, its potential benefits, risks, and alternatives, and provides them with the opportunity to make an informed decision about their participation or treatment.
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Informed consent is a process used in healthcare to provide patients with information on the risks and benefits of a medical procedure or treatment so they can make an informed decision.
Healthcare providers are required to obtain informed consent from patients before performing any medical procedure or treatment.
To fill out informed consent, healthcare providers must ensure that patients understand the information provided, discuss any questions or concerns, and obtain the patient's signature to indicate their agreement.
The purpose of informed consent is to protect the patient's autonomy and right to make decisions about their own healthcare.
Informed consent forms must include a description of the procedure or treatment, risks and benefits, alternative options, and the patient's right to refuse treatment.
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