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Protocol Review & Monitoring System (PRMS)Scientific Review Committee (SRC) Policies and Procedures Fred & Pamela Buffett Cancer CenterVersion 13.0, 09/09/2024 1|P a g eCONTACT INFORMATION ASSOCIATE
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How to fill out protocol review amp monitoring

How to fill out protocol review amp monitoring
01
Review the protocol guidelines to ensure compliance with ethical standards.
02
Prepare a summary of your research objectives and methodology.
03
Complete the protocol review application form, providing all required details.
04
Attach relevant documents, such as informed consent forms and recruitment materials.
05
Submit the application to the designated review board for evaluation.
06
Address any feedback or required modifications from the review board.
07
Once approved, proceed with monitoring the study as per the protocol.
Who needs protocol review amp monitoring?
01
Researchers conducting clinical trials or studies involving human subjects.
02
Institutions seeking to maintain ethical standards in research.
03
Funding agencies requiring assurance of protocol compliance.
04
Participants wishing to understand the oversight and safety measures in research.
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What is protocol review amp monitoring?
Protocol review and monitoring is a process where proposed research protocols are reviewed to ensure they meet ethical, legal, and scientific standards before being approved and monitored throughout the study to ensure compliance and safety.
Who is required to file protocol review amp monitoring?
Researchers and institutions conducting studies that involve human subjects, animal subjects, or sensitive data are typically required to file for protocol review and monitoring.
How to fill out protocol review amp monitoring?
To fill out a protocol review and monitoring application, researchers must provide detailed information about the study design, objectives, methodology, potential risks, data management plans, and consent procedures.
What is the purpose of protocol review amp monitoring?
The purpose of protocol review and monitoring is to protect the rights and welfare of participants, ensure scientific integrity, and comply with regulatory requirements throughout the research process.
What information must be reported on protocol review amp monitoring?
Key information that must be reported includes study objectives, research design, participant recruitment methods, risk assessment, data handling procedures, and ethical considerations.
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