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This document outlines the procedures and requirements for submitting a research protocol for review by the Human Subjects Review Committee at Wilmington College. It includes sections for investigator
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How to fill out hsrc protocol review form

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How to fill out HSRC Protocol Review Form

01
Obtain the HSRC Protocol Review Form from the official HSRC website or office.
02
Fill in the project title at the top of the form.
03
Provide the names and contact information of the principal investigator and co-investigators.
04
Clearly outline the study objectives and research questions.
05
Describe the study design, including methodology and data collection techniques.
06
Include details on participant recruitment and selection criteria.
07
Address potential risks to participants and how they will be mitigated.
08
Specify plans for data management and confidentiality measures.
09
Add any funding sources and ethical considerations.
10
Review the form for completeness and accuracy before submission.

Who needs HSRC Protocol Review Form?

01
Researchers conducting studies involving human participants.
02
Institutional review boards evaluating research protocols.
03
Ethical committees assessing compliance with research standards.
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The HSRC Protocol Review Form is a document used to submit research proposals for ethical review by the Human Subject Research Committee (HSRC) to ensure the protection of participants' rights and welfare.
All researchers, including faculty, students, and staff who are conducting research involving human subjects, are required to file the HSRC Protocol Review Form.
The HSRC Protocol Review Form should be completed by providing detailed information about the research project, including objectives, methodology, participant recruitment, informed consent process, and potential risks and benefits.
The purpose of the HSRC Protocol Review Form is to evaluate the ethical considerations and regulatory compliance of research involving human subjects to ensure their safety and rights are protected.
The form must include information such as the study title, principal investigator details, research objectives, participant demographics, data collection methods, consent procedures, and any risks associated with the research.
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