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SUN College at Neon Animal Care and Use Protocol Please complete all the appropriate sections of this form and send an electronic copy to IACUC@oneonta.edu. Note that within one year of approval of

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How to fill out new protocol review form

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Obtain a blank copy of the new protocol review form

02

Fill in all required information such as research title, investigator name, contact information, and study procedures

03

Provide a detailed description of the research objectives and methodology

04

Include any relevant information on risks and benefits to participants

05

Obtain necessary signatures from co-investigators, department heads, and any other required parties

06

Submit the completed form to the appropriate review board for approval

Who needs new protocol review form?

01

Researchers or investigators planning to conduct a new research study that involves human participants typically need to fill out a new protocol review form. This form helps ensure that the research is ethically conducted and compliant with regulations.

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What is new protocol review form?

The new protocol review form is a document used to propose and evaluate a new research study involving human subjects.

Who is required to file new protocol review form?

Researchers and institutions conducting research studies involving human subjects are required to file a new protocol review form.

How to fill out new protocol review form?

The new protocol review form can be filled out online or submitted in hard copy with all required information about the research study and its potential impact on human subjects.

What is the purpose of new protocol review form?

The purpose of the new protocol review form is to ensure that research studies involving human subjects are conducted ethically and in compliance with regulations to protect the rights and welfare of the participants.

What information must be reported on new protocol review form?

The new protocol review form must include details about the research study design, methodology, potential risks and benefits to participants, informed consent process, and any safeguards in place to protect participants.

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