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IRB Office use only Date submitted___BU Charles River IRB Application Form (Exempt) SECTION A: PROTOCOL AND CONTACT INFORMATION Protocol Number (To be assigned by IRB Office): Protocol Title: Principal
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How to fill out bu charles river irb
How to fill out bu charles river irb
01
Step 1: Log in to the Charles River IRB website.
02
Step 2: Navigate to the 'Forms' section.
03
Step 3: Select the appropriate form for filling out the BU Charles River IRB.
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Step 4: Review the instructions and guidelines provided for the form.
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Step 5: Fill out the form accurately and completely, providing all necessary information.
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Step 6: Double-check the form for any errors or omissions.
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Step 7: Submit the completed form through the designated submission method.
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Step 8: Wait for confirmation or feedback from the Charles River IRB.
Who needs bu charles river irb?
01
Researchers conducting studies involving human subjects.
02
Individuals or organizations seeking ethical approval for research involving human subjects.
03
Institutions or universities requiring IRB approval for research projects.
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What is bu charles river irb?
BU Charles River IRB refers to the Institutional Review Board at Boston University that oversees research involving human subjects to ensure ethical standards are met.
Who is required to file bu charles river irb?
Researchers and faculty members at Boston University conducting studies involving human subjects are required to file with the BU Charles River IRB.
How to fill out bu charles river irb?
To fill out the BU Charles River IRB application, researchers must complete an online submission form detailing the research protocol, participant recruitment, informed consent process, and risk assessment.
What is the purpose of bu charles river irb?
The purpose of the BU Charles River IRB is to protect the rights and welfare of human subjects involved in research by reviewing study proposals for ethical compliance.
What information must be reported on bu charles river irb?
Researchers must report detailed information including study objectives, methodologies, participant populations, potential risks, benefits, consent procedures, and data protection measures.
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