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Millikan University IRB Consent Form Instructions The purpose of obtaining informed consent is to provide participants with information they can easily understand allowing them to accurately weigh
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Reference-informed consent guidelines refer to a set of rules and procedures that ensure individuals are properly informed before consenting to participate in a study or research project.
Researchers, scientists, and institutions conducting studies or research projects are usually required to file reference-informed consent guidelines.
Reference-informed consent guidelines can be filled out by providing detailed information about the study, risks involved, benefits, and procedures, ensuring that participants fully understand what they are consenting to.
The purpose of reference-informed consent guidelines is to protect the rights and well-being of research participants by ensuring that they are fully informed and able to make a voluntary decision to participate.
Reference-informed consent guidelines must include details about the study objectives, procedures, risks, benefits, confidentiality, participant rights, and contact information for questions or concerns.
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