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IRB #: STU00207397MODCR0001 Approved by NU IRB for use on or after 4/9/2019Consent to Participate in Research Page 1 of 6Title of Research Study: Feasibility of Oncology to Improve Self-management
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How to fill out initial irb review of
How to fill out initial irb review of
01
Obtain the initial IRB application form from the institution's IRB office.
02
Fill out the form with accurate and detailed information about the research study, including the study objectives, methods, risks, and benefits.
03
Include any additional documentation required by the IRB, such as informed consent forms, recruitment materials, and study protocols.
04
Submit the completed application form and supporting documents to the IRB office for review.
05
Respond promptly to any requests for additional information or clarification from the IRB reviewers.
Who needs initial irb review of?
01
Researchers conducting human subjects research at institutions that have an IRB committee in place.
02
Students conducting research projects involving human subjects as part of their academic studies.
03
Healthcare professionals seeking to conduct research involving human participants.
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What is initial irb review of?
The initial IRB review is the first review conducted by an Institutional Review Board (IRB) to evaluate the ethics of a research study involving human subjects.
Who is required to file initial irb review of?
Researchers conducting a research study involving human subjects are required to file for initial IRB review.
How to fill out initial irb review of?
To fill out the initial IRB review, researchers must provide detailed information about the study protocol, informed consent process, potential risks and benefits, and measures to protect participant confidentiality.
What is the purpose of initial irb review of?
The purpose of the initial IRB review is to ensure that research involving human subjects is conducted ethically and in compliance with regulations and guidelines.
What information must be reported on initial irb review of?
The initial IRB review must include information on the study protocol, informed consent process, potential risks and benefits, and measures to protect participant confidentiality.
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