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Received by the NMDP IRB 04/18/2024 CHLA CONSENT FORM STANDARDS AND REQUIRED CONSENT LANGUAGE WHEN RELYING ON THE NMDP IRB This document provides: 1. General Instructions about how to prepare and
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What is easy-to-read informed consent forms?
Easy-to-read informed consent forms are documents that are written in a clear and simple language, making it easy for individuals to understand the information provided.
Who is required to file easy-to-read informed consent forms?
Researchers, medical professionals, and institutions conducting studies or providing medical treatments are required to file easy-to-read informed consent forms.
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Easy-to-read informed consent forms can be filled out by providing all required information in a clear and concise manner, ensuring that the participant understands the purpose of the study or treatment, risks involved, and their rights.
What is the purpose of easy-to-read informed consent forms?
The purpose of easy-to-read informed consent forms is to ensure that individuals are fully informed about the study or treatment they are participating in, including the risks involved, their rights, and any potential benefits.
What information must be reported on easy-to-read informed consent forms?
Easy-to-read informed consent forms must include information about the purpose of the study or treatment, potential risks and benefits, participant rights, confidentiality, and contact information for questions or concerns.
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