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APPROVED BY THE YALE UNIVERSITY IRB 4/6/2021YALE UNIVERSITY SCHOOL OF MEDICINE Alone Haven Hospital & Saint Raphael Campus Yale New Haven Health Network Greenwich Hospital Yale New Haven Health Network

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How to fill out human research protection program

01

Obtain necessary training in human subjects research ethics

02

Familiarize yourself with the regulations and guidelines applicable to human research protection

03

Complete all required documentation for the protocol, including informed consent forms

04

Implement strategies to ensure participant confidentiality and privacy

05

Obtain approval from the Institutional Review Board (IRB) before commencing the research

Who needs human research protection program?

01

Researchers conducting studies involving human subjects

02

Institutions or organizations conducting research involving human subjects

03

Funding agencies that support research involving human subjects

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What is human research protection program?

The human research protection program is a set of procedures and guidelines designed to ensure the safety, well-being, and rights of individuals participating in research studies.

Who is required to file human research protection program?

Institutional review boards (IRBs) and researchers conducting human subjects research are required to file a human research protection program.

How to fill out human research protection program?

To fill out a human research protection program, researchers must provide detailed information about their research study, the potential risks and benefits to participants, and the steps taken to protect participants' rights and confidentiality.

What is the purpose of human research protection program?

The purpose of the human research protection program is to ensure that research involving human subjects is conducted ethically and in compliance with regulations to protect the rights and welfare of participants.

What information must be reported on human research protection program?

Information that must be reported on a human research protection program includes the study protocol, informed consent forms, recruitment materials, and procedures for data collection and analysis.

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