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Get the free HRPP Policy 445: Use of Stored Data and Biological Specimens in Human Research - yale

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This policy outlines the requirements for the use of stored data and biological specimens in human research at Yale University, including the necessity of Institutional Review Board (IRB) approval,
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How to fill out HRPP Policy 445: Use of Stored Data and Biological Specimens in Human Research

01
Read HRPP Policy 445 to understand its purpose and scope.
02
Gather all necessary stored data and biological specimens that will be used in human research.
03
Ensure compliance with ethical guidelines and regulations regarding human subjects.
04
Complete the required forms as specified in the policy.
05
Review and document consent processes for participants regarding their data and specimens.
06
Submit the completed documents to the appropriate HRPP committee for review.
07
Make any requested revisions based on feedback from the HRPP committee.
08
Obtain final approval before proceeding with research activities.

Who needs HRPP Policy 445: Use of Stored Data and Biological Specimens in Human Research?

01
Researchers conducting studies involving human subjects.
02
Institutional Review Board (IRB) members overseeing research ethics.
03
Data managers handling stored data and biological specimens.
04
Compliance officers ensuring adherence to regulations and policies.
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HRPP Policy 445 outlines the guidelines and requirements for the use of stored data and biological specimens in human research to ensure ethical and responsible research practices.
All researchers who intend to use stored data or biological specimens for human research must file HRPP Policy 445.
To fill out HRPP Policy 445, researchers must provide detailed information about their research proposal, including the sources of stored data and specimens, their intended use, and how participant consent will be obtained or managed.
The purpose of HRPP Policy 445 is to ensure the protection of human subjects' rights and welfare while facilitating the responsible use of previously collected data and biological specimens.
Researchers must report information including the type of data or specimens being used, the origin of these materials, the research objectives, ethical considerations, and details about participant consent.
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