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Permission to Take Part in a Human Research Studying version number: [insert ICF version number] Title of research study1: [insert title of research study here with protocol number, if applicable]
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01
Open the HRPP Toolkit Protocol Templates on your computer
02
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03
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04
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05
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Who needs hrpp toolkit protocol templates?

01
Researchers conducting human subjects research
02
Institutional Review Boards (IRBs)
03
Ethics committees
04
Research compliance offices
05
Any individual or organization involved in the development or review of research protocols

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The HRPP Toolkit Protocol Templates are standardized documents used for preparing and submitting research protocols that ensure compliance with ethical and regulatory standards in human research.
Researchers conducting studies involving human subjects are required to file HRPP Toolkit Protocol Templates as part of the ethical review process.
To fill out HRPP Toolkit Protocol Templates, researchers should provide detailed information about the study's purpose, design, methodology, informed consent process, and any potential risks to participants.
The purpose of HRPP Toolkit Protocol Templates is to promote consistency, clarity, and compliance in the submission of research protocols, aiding ethical review and oversight.
Information that must be reported includes the study title, objectives, study design, participant selection criteria, recruitment methods, data collection procedures, and risk assessment.
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