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Study Termination Form for studies approved by theology General Hospital Research Ethics CommitteePlease complete form and return to the Research Ethics Committee Administrator, SGH1. Principal Investigator:2.
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An easy-to-read informed consent form is a simplified document that outlines the nature, risks, and benefits of a procedure or research study in clear language that is accessible to individuals without technical expertise.
Researchers and organizations conducting clinical trials or studies that involve human participants are required to file an easy-to-read informed consent form.
To fill out an easy-to-read informed consent form, you should provide clear information about the study, including its purpose, procedures, risks, benefits, and participant rights, using simple and straightforward language.
The purpose of an easy-to-read informed consent form is to ensure that participants understand the nature of the study and voluntarily agree to participate based on informed and clear information.
The easy-to-read informed consent form must report information about the study's purpose, procedures, potential risks, benefits, confidentiality measures, compensation, and the right to withdraw from the study.
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