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HUNTER COLLEGE OF THE CITY UNIVERSITY OF NEW YORK VIDEO RECORDING RELEASE CONSENT FORM Protocol #: Researcher(s): Title: As part of this project, a video recording will be made of you during your

How to fill out cuny irb - hunter

How to fill out CUNY IRB?

1. Start by accessing the CUNY IRB portal. Visit the official website and look for the IRB section or the specific page for submitting IRB applications.
2. Create an account or login if you already have one. Typically, you will need to provide basic information such as your name, email address, and affiliation with CUNY.
3. Read and familiarize yourself with the guidelines, policies, and procedures for CUNY IRB. It is crucial to understand the requirements and ethical considerations before proceeding with your application.
4. Determine the type of application you need to submit. CUNY IRB usually offers different application forms based on the nature of your research, such as full board review, expedited review, or exempt review. Select the appropriate form for your study.
5. Fill out the application form carefully and accurately. Provide all the necessary information, including your research protocol, study design, participant recruitment methods, data collection procedures, and any potential risks or benefits. Be thorough and clear in your responses.
6. Include all the required supporting documents. Depending on the nature of your research, you may need to attach documents such as informed consent forms, questionnaires, surveys, or letters of support from collaborating institutions or researchers.
7. Review your application before submission. Double-check for any errors, incomplete sections, or missing documents. It is essential to present a well-prepared and organized application to expedite the review process.
8. Submit your application through the designated online submission portal. Follow the instructions provided, and ensure that you have included all the necessary documents and information.

Who needs CUNY IRB?

1. Researchers conducting human subjects research at City University of New York (CUNY) campuses or affiliated institutions are required to obtain approval from the CUNY Institutional Review Board (IRB).
2. Faculty members, graduate students, undergraduate students, and any individuals affiliated with CUNY who plan to involve human participants in their research must comply with the CUNY IRB process.
3. Even if your research is conducted outside of CUNY facilities, if you are affiliated with CUNY and plan to involve human subjects, it is essential to go through the CUNY IRB for the necessary ethical review and approval.
4. Studies that fall under the federal regulations for human subjects research, such as those funded by federal agencies like the National Institutes of Health (NIH), require CUNY IRB approval.
5. It is important to note that some research activities may be exempt from the full IRB review process but still need to undergo an expedited or exempt review by the CUNY IRB to ensure compliance with ethical guidelines.

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What is cuny irb?

CUNY IRB stands for City University of New York Institutional Review Board, which oversees research involving human subjects conducted by CUNY faculty, staff, and students.

Who is required to file cuny irb?

All CUNY faculty, staff, and students who are conducting research involving human subjects are required to file with the CUNY IRB.

How to fill out cuny irb?

To fill out the CUNY IRB, researchers need to submit an application detailing their research project, including information about the study design, methods, risks to participants, and informed consent procedures.

What is the purpose of cuny irb?

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

What information must be reported on cuny irb?

Researchers must report detailed information about their research project, including the study design, methods, risks to participants, informed consent procedures, and any potential conflicts of interest.