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Altru Health System Human Subjects Review Form 2010 free printable template

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Institutional Review Board Human Subjects Review Form For new projects or procedural revisions to approved projects involving human subjects. Date: Principal Investigator: Address to which notice
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How to fill out Altru Health System Human Subjects Review Form

01
Begin by downloading the Altru Health System Human Subjects Review Form from the official website.
02
Carefully read the accompanying guidelines to understand the requirements.
03
Fill out the applicant information section, including name, contact information, and affiliation.
04
Provide a detailed description of the research project, including its purpose, methodology, and intended outcomes.
05
Clearly outline any potential risks to participants and how these will be mitigated.
06
Include information about informed consent and how it will be obtained from participants.
07
Answer any specific questions related to the ethical considerations of the research.
08
Review the form for completeness and accuracy before submission.
09
Submit the completed form to the appropriate review committee as specified in the guidelines.

Who needs Altru Health System Human Subjects Review Form?

01
Researchers conducting studies involving human subjects at Altru Health System.
02
Students or academic professionals seeking approval for research projects.
03
Organizations or companies planning to conduct clinical trials or similar studies.
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The Altru Health System Human Subjects Review Form is a document used to evaluate research proposals involving human subjects to ensure ethical standards and protect participant rights.
Researchers and investigators who plan to conduct studies involving human subjects at Altru Health System are required to file this form.
To fill out the form, researchers must provide detailed information about their study, including objectives, methodology, participant recruitment, informed consent processes, and potential risks to participants.
The purpose of the form is to ensure compliance with ethical guidelines and regulations in research involving human subjects, protecting their welfare and rights.
The form must report information such as study title, research questions, participant criteria, data collection methods, risks and benefits, and how informed consent will be obtained.
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