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Informed Consent Form for Parents/Guardians of Subjects Do probiotics modulate the intestinal microbiome in extremely premature infants? Principal Investigator: Dr. Harish Amino REB160542 Version
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Read the informed consent form thoroughly to understand its purpose and requirements.
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Who needs informed consent form for?

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Informed consent forms are typically required from individuals who are participating in medical research studies, clinical trials, or experimental treatments.
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Healthcare professionals may also require patients to fill out informed consent forms before certain medical procedures or treatments.
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Informed consent is essential whenever there is a need to ensure that individuals understand the risks, benefits, and alternatives associated with a particular decision or course of action.
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Various industries, such as education and legal services, may also have specific situations where informed consent forms are necessary.
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The specific requirements for who needs an informed consent form may vary depending on the country, organization, or specific context.
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The informed consent form is used to ensure that participants in a study or medical treatment understand the risks and benefits before agreeing to participate.
Researchers, medical professionals, or anyone conducting a study or treatment involving human subjects.
The form should be filled out by providing clear information about the study or treatment, risks and benefits, and obtaining the participant's signature to indicate their consent.
The purpose of the informed consent form is to protect the rights and well-being of participants in a study or medical treatment.
The form must include details about the study or treatment, risks and benefits, confidentiality, contact information, and participant's rights.
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