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This document serves as a consent form for participants in a research study focused on the collection of anti-influenza A H1N1 immune plasma. It outlines the study's purpose, procedures, risks, benefits,
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How to fill out University of Pennsylvania Health System IRB Approval

01
Visit the University of Pennsylvania Health System IRB website.
02
Review the guidelines and policies for IRB submissions.
03
Prepare your research protocol including objectives, methods, and participant details.
04
Complete the IRB application form provided on the website.
05
Gather all required documents such as consent forms, recruitment materials, and data collection instruments.
06
Submit the completed application and documents via the online IRB submission system.
07
Monitor the status of your submission and respond to any requests for additional information or revisions from the IRB.
08
Attend the IRB meeting if necessary to discuss your application.

Who needs University of Pennsylvania Health System IRB Approval?

01
Researchers conducting studies involving human subjects at the University of Pennsylvania Health System.
02
Faculty, staff, and students involved in any research project that requires data collection from individuals.
03
Any organization or individual collaborating with the University of Pennsylvania Health System on research projects involving human subjects.
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There are three levels of IRB review: exempt, expedited , and convened.
UPHS and the Perelman School of Medicine at the University of Pennsylvania together comprise Penn Medicine, a clinical and research entity of the University of Pennsylvania.
If you have questions, you can call the Einstein Institutional Review Board. Their number is 718-430-2237.
If you require faster assistance, please call the IRB mainline at 215-573-2540. Please note that the IRB does not have time nor resources to provide 1-on-1 walkthroughs of the online submission system. If you need this type of assistance, please sign up for an IRB 101 session.

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University of Pennsylvania Health System IRB Approval is a formal authorization from the Institutional Review Board (IRB) that ensures research involving human subjects meets ethical standards and complies with regulatory requirements.
All researchers, faculty, and students conducting any research involving human subjects at the University of Pennsylvania Health System are required to file for IRB Approval.
To fill out the University of Pennsylvania Health System IRB Approval, researchers must complete the required application forms available on the IRB's website, provide detailed information about the research protocol, and submit any necessary consent documents.
The purpose of University of Pennsylvania Health System IRB Approval is to protect the rights and welfare of human subjects involved in research by ensuring ethical practices and compliance with federal regulations.
The information that must be reported includes the research objectives, study design, participant recruitment plans, informed consent process, potential risks and benefits, and data confidentiality measures.
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