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20172042 IRB Approved at the Protocol Level Sep 13, 2018PROTOCOL Clinical Investigation of New CI Delivery Models in a Nucleus CI Population Version 2.0 August 2018 Study Sponsor Cochlear Americas
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To fill out the IRB approved AT form, follow these steps:
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Start by reading the instructions provided on the form.
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Provide your name, contact information, and affiliation with the institution conducting the research.
04
Clearly state the purpose of the research and describe the methodology you will be using.
05
If there are any potential risks or discomforts to the participants, make sure to mention them and explain how you plan to minimize these risks.
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Provide a detailed explanation of how you will obtain informed consent from the participants and ensure their privacy and confidentiality.
07
Describe the recruitment process for selecting participants and explain any incentives, if applicable.
08
Include a section where you outline the data collection methods and instruments you will be using.
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Indicate how you will store and secure the collected data to protect the participants' confidentiality.
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If applicable, provide details on any debriefing or follow-up procedures you plan to conduct.
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Double-check all the information filled out on the form for accuracy and completeness before submitting it to the IRB for approval.

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The IRB approved AT form is required for individuals or organizations conducting research involving human subjects.
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This includes researchers in academic institutions, government agencies, or private organizations.
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It ensures that the research is conducted ethically and in compliance with relevant regulations and guidelines.
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The IRB Approved At form is a document used to confirm that a research study has received approval from an Institutional Review Board (IRB) before it begins.
Researchers or institutions conducting studies that involve human subjects are required to file the IRB Approved At form.
To fill out the IRB Approved At form, provide details such as the study title, IRB approval date, researcher information, and any conditions of the approval.
The purpose of the IRB Approved At form is to ensure compliance with ethical standards in research involving human subjects, confirming that proper review and approval have taken place.
The form must report the study title, IRB approval number, approval date, names of principal investigators, and any changes required for the study.
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