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USES INSTITUTIONAL REVIEW BOARD APPLICATION FOR INITIAL REVIEW OF HUMAN SUBJECTS RESEARCH January 2023 Name of Principal Investigator (PI) ___ Phone___ (Faculty/Staff) PI credentials (rank and highest

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How to fill out umes institutional review board

01

Obtain the necessary forms from the UMES Institutional Review Board office.

02

Fill out the required information including project title, investigator information, study protocol, consent form, and any other relevant details.

03

Submit the completed forms along with any supporting documents to the IRB office for review.

04

Address any feedback or revisions requested by the IRB panel.

05

Once approved, adhere to the guidelines and regulations set forth by the IRB while conducting the research.

Who needs umes institutional review board?

01

Researchers conducting studies involving human subjects at the University of Maryland Eastern Shore (UMES) need to obtain approval from the UMES Institutional Review Board.

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What is umes institutional review board?

The UMES Institutional Review Board (IRB) is a committee responsible for reviewing and approving research involving human subjects at the University of Maryland Eastern Shore (UMES).

Who is required to file umes institutional review board?

Researchers conducting studies involving human subjects at UMES are required to file an application with the Institutional Review Board.

How to fill out umes institutional review board?

To fill out the UMES Institutional Review Board application, researchers must provide detailed information about their study protocol, recruitment methods, risks and benefits to participants, and informed consent procedures.

What is the purpose of umes institutional review board?

The purpose of the UMES Institutional Review Board 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 umes institutional review board?

Researchers must report information such as study protocols, recruitment methods, risks and benefits to participants, informed consent procedures, and any potential conflicts of interest.

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