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BRI MODEL PHONE SCRIPT TEMPLATE ELECTRONIC INFORMED CONSENT This template should be used when conducting the consent process over the phone with an electronic informed consent form (i.e. Adobe Sign).
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To fill out the researchwayneeduirbinformed-consenttemplates and guidance, follow these steps:
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Start by reading the provided instructions carefully.
03
Begin with the participant's personal information, including their name, age, and contact details.
04
Clearly state the purpose of the research and provide a brief overview of the study.
05
Explain the procedures that will be involved in the research and any potential risks or benefits.
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Clearly outline the voluntary nature of participation and emphasize that the participant can withdraw at any time.
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Describe the confidentiality and data protection measures that will be implemented.
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Provide a space for the participant or their legal representative to sign and date the consent form.
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Make sure to include any additional information or requirements specific to your research project.
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Be sure to review and double-check the completed form for any errors or missing information before finalizing it.
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Keep a copy of the signed consent form for your records.

Who needs researchwayneeduirbinformed-consenttemplates and guidance for?

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Researchwayneeduirbinformed-consenttemplates and guidance are needed by researchers, research institutions, or anyone conducting studies involving human participants.
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It is essential to obtain informed consent from participants to ensure ethical compliance and protect the rights and welfare of individuals involved in the research.
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Researchers conducting clinical trials, surveys, experiments, or any other form of research that involves human subjects should use informed consent templates and follow guidance to ensure a standardized and ethical approach.

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Researchwayneeduirbinformed-consenttemplates and guidance provide a standard template and instructions for obtaining informed consent from research participants.
Researchers and institutions conducting research involving human subjects are required to file researchwayneeduirbinformed-consenttemplates and guidance.
Researchers must carefully follow the instructions provided in the template and accurately fill out all required information.
The purpose is to ensure that research participants are fully informed about the study, its risks and benefits, and have given voluntary consent to participate.
Information such as study title, purpose, procedures, risks, benefits, confidentiality, and contact information must be reported on the templates.
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