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Submission#: 352958 IORG0000196 BORG#: U of Pittsburgh Institution:OMB No. 09900279 Approved for use through October 31, 2018U. S. Department of Health and Human Services (HHS) Registration of an

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How to fill out irb registration instructionshhsgovirb registration

01

Go to the IRB registration website of HHSGov.

02

Create an account with a valid email address.

03

Fill out the required information such as your name, institution, and research project details.

04

Submit the completed form for review and approval.

Who needs irb registration instructionshhsgovirb registration?

01

Researchers conducting studies involving human subjects need IRB registration instructions from HHSGov.

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What is irb registration instructionshhsgovirb registration?

IRB registration instructions refer to the guidelines set by the institutional review board (IRB) regarding the registration of studies involving human subjects. This process ensures compliance with ethical standards and regulations.

Who is required to file irb registration instructionshhsgovirb registration?

Any institution or organization conducting research involving human subjects must file for IRB registration to ensure ethical oversight. This includes universities, hospitals, and private research firms.

How to fill out irb registration instructionshhsgovirb registration?

To fill out the IRB registration, you must provide detailed information about the research study, including the study title, the principal investigator, a description of the research, and information regarding subjects involved.

What is the purpose of irb registration instructionshhsgovirb registration?

The purpose of IRB registration is to protect the rights and welfare of human subjects involved in research, ensuring that studies are conducted ethically and in compliance with federal regulations.

What information must be reported on irb registration instructionshhsgovirb registration?

The registration must report details such as the research title, description of the study, principal investigator's name, institutional affiliation, and the consent process for participants.

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