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Mostrecentrevision:05/28/2020|01/07/2020|Original:07/15/11VALENCIACOLLEGE HumanResearchProtection(HIP)InstitutionalReviewBoard(IRB) TheValenciaIRBOverviewandApplicationPackageforResearchersPrimaryInvestigators(PI's)
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How to fill out valencia college irb overview
How to fill out valencia college irb overview
01
Visit the Valencia College IRB website
02
Click on the 'IRB Overview' link
03
Read through the information provided on the overview page
04
Fill out the required sections with accurate information
05
Submit the completed overview form as per the instructions on the website
Who needs valencia college irb overview?
01
Researchers conducting studies involving human subjects at Valencia College
02
Students conducting research projects that require IRB approval
03
Faculty members supervising research projects involving human subjects
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What is valencia college irb overview?
Valencia College's Institutional Review Board (IRB) overview provides guidelines for researchers conducting studies involving human subjects, ensuring ethical standards and compliance with federal regulations.
Who is required to file valencia college irb overview?
All faculty, staff, and students at Valencia College who are involved in research projects that involve human subjects are required to file the IRB overview.
How to fill out valencia college irb overview?
To fill out the Valencia College IRB overview, researchers must complete the IRB application form, provide necessary documentation including study protocols and consent forms, and submit it for review through the college's IRB submission portal.
What is the purpose of valencia college irb overview?
The purpose of the Valencia College IRB overview is to protect the rights and welfare of human subjects involved in research, ensuring ethical conduct and compliance with applicable laws and regulations.
What information must be reported on valencia college irb overview?
The IRB overview must report detailed information about the research study, including objectives, methodology, participant information, informed consent processes, and potential risks and benefits.
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