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This document outlines the application process for certification of Honest Broker Systems/Processes within the UPMC Health System and University of Pittsburgh, detailing the roles and responsibilities,
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How to fill out UPMC Health System/University of Pittsburgh Institutional Review Board Application

01
Begin by gathering all necessary information related to your research project.
02
Complete the online application form on the UPMC Health System/University of Pittsburgh IRB website.
03
Provide a brief summary of your research, including its purpose and significance.
04
Describe the study design, including methodology and participant recruitment strategies.
05
Outline any potential risks to participants and how you plan to mitigate them.
06
Explain how you will obtain informed consent from participants.
07
Include details about data collection and storage methods, ensuring participant confidentiality.
08
Review the application for completeness and accuracy before submission.
09
Submit the application and note any required documentation or supplementary materials.
10
Be prepared to respond to any queries or revisions requested by the IRB.

Who needs UPMC Health System/University of Pittsburgh Institutional Review Board Application?

01
Researchers at UPMC or the University of Pittsburgh planning to conduct studies involving human subjects.
02
Students conducting thesis or dissertation research that requires ethical approval.
03
Faculty members initiating clinical trials or other research projects that involve direct interaction with participants.
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The UPMC Health System/University of Pittsburgh Institutional Review Board Application is a formal request for approval to conduct research involving human subjects, ensuring compliance with ethical standards and regulatory requirements.
Researchers affiliated with UPMC or the University of Pittsburgh planning studies that involve human participants must file the application.
The application is filled out by providing detailed information about the study design, methodology, participant recruitment, informed consent processes, and any potential risks to participants.
The purpose of the application is to protect the rights and welfare of human subjects in research by ensuring that all studies adhere to ethical guidelines and regulatory standards.
The application requires reporting information such as study objectives, research methods, participant demographics, consent procedures, risk assessments, and data handling protocols.
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