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Human Research Protections Program#150428Approved Current Approval: Do not use after05/05/2015 05/03/2016Pages 5University of California, San Diego Consent to Act as a Research SubjectSTUDY TITLE

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How to fill out human research protection program

01

Familiarize yourself with the guidelines and regulations for human research protection program (HRPP) set by federal and institutional policies.

02

Obtain necessary training and certification in human subjects protection.

03

Submit an application for review to the institutional review board (IRB) outlining your research protocol, risks and benefits, and informed consent process.

04

Address any feedback or revisions requested by the IRB before proceeding with your research.

05

Continuously monitor and report any adverse events or updates to the IRB throughout the duration of your study.

06

Renew your HRPP approval as required by your institution's policies and regulations.

Who needs human research protection program?

01

Researchers conducting studies involving human subjects.

02

Institutions and organizations conducting research involving human participants.

03

Students conducting research as part of their academic coursework or thesis.

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What is human research protection program?

A human research protection program is a set of policies and procedures designed to ensure the rights and welfare of individuals participating in research studies.

Who is required to file human research protection program?

Institutions conducting research involving human subjects are required to have and file a human research protection program.

How to fill out human research protection program?

To fill out a human research protection program, institutions must establish guidelines for the ethical conduct of research involving human subjects, obtain approval from an institutional review board, and adhere to applicable regulations.

What is the purpose of human research protection program?

The purpose of a human research protection program is to safeguard the rights, safety, and well-being of individuals participating in research studies.

What information must be reported on human research protection program?

Information that must be reported on a human research protection program includes the protocol for the research study, risks and benefits to participants, consent forms, and procedures for monitoring and reporting adverse events.

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