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CASE STUDY CONSENT FORM1 Use this to get patients consent to publish their images and/or information in The Hearing Journal. Medical practitioner or corresponding author(s): Name of patient described
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01
Obtain the case study consent form from the relevant department or organization.
02
Ensure all relevant sections of the form are completed including participant information, study details, and signatures from both the participant and researcher.
03
Provide the participant with a clear explanation of the study purpose, procedures, risks, and benefits before asking them to sign the form.
04
Address any questions or concerns the participant may have about the study before obtaining their consent.
05
Keep a copy of the signed consent form on file for record-keeping purposes.

Who needs case study consent form1?

01
Researchers conducting case studies that involve human participants require the case study consent form to ensure ethical standards are met and participants are fully informed and willing to take part in the study.
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Case study consent form1 is a document that outlines the terms and conditions for participating in a research study.
Anyone participating in the research study is required to file the case study consent form1.
To fill out the case study consent form1, one must carefully read and follow the instructions provided on the form.
The purpose of the case study consent form1 is to ensure that participants understand the risks and benefits of participating in the research study and to obtain their informed consent.
The case study consent form1 must include information about the research study, the risks and benefits of participation, the participant's rights, and any compensation or incentives offered.
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