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Milwaukee Area Technical College REQUEST FOR INSTITUTIONAL REVIEW BOARD ACTIONShaded areas of this form are for IRB use only1. PROJECT INFORMATION:Investigator name: ___ Date: ___Email: ___ Phone
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How to fill out coordinated irb review request

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How to fill out coordinated irb review request

01
Obtain the Coordinated IRB Review Request form from the IRB office or website.
02
Fill out the required information on the form, including study title, principal investigator information, and study objectives.
03
Provide a brief summary of the research protocol, including the study design and procedures involved.
04
Include any relevant documentation such as study protocols, consent forms, and participant recruitment materials.
05
Submit the completed form and any accompanying documents to the IRB office for review.

Who needs coordinated irb review request?

01
Researchers who are conducting collaborative research involving multiple institutions or sites that require IRB approval from each participating institution.

What is COORDINATED IRB REVIEW REQUEST Introduction Form?

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COORDINATED IRB REVIEW REQUEST Introduction template instructions

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A coordinated IRB review request is a submission made to multiple Institutional Review Boards (IRBs) to seek ethical approval for a multi-site research study, ensuring that all participating sites are operating under the same ethical guidelines.
Researchers conducting studies that involve multiple institutions or sites require a coordinated IRB review request to streamline the ethical review process across all entities involved.
To fill out a coordinated IRB review request, researchers should complete a standard application form that includes details about the study, its methodology, participant information, and consent processes, and ensure that required documents are attached.
The purpose of a coordinated IRB review request is to facilitate the ethical approval process for multi-site studies, reduce redundancy in reviews, and ensure consistent application of ethical standards across locations.
The coordinated IRB review request must include the study title, research objectives, procedural details, participant demographics, informed consent processes, data collection methods, and any potential risks to participants.
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