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This document serves as a signature page for investigators applying for grant proposals involving human subjects research, ensuring compliance with IRB requirements.
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How to fill out just-in-time human subjects review

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How to fill out Just-in-Time Human Subjects Review Grant Application Signature Page

01
Gather necessary documents including the grant application and any required supporting materials.
02
Locate the Signature Page of the Just-in-Time Human Subjects Review Grant Application.
03
Identify the principal investigator and other co-investigators who need to sign the page.
04
Ensure that all involved parties have their contact information ready, including email addresses and telephone numbers.
05
Fill in the date of submission for the application.
06
Sign the Signature Page in the designated areas for each investigator.
07
Collect all signatures and ensure that there are no missing entries.
08
Submit the signed Signature Page along with your grant application as per the submission guidelines.

Who needs Just-in-Time Human Subjects Review Grant Application Signature Page?

01
Research teams that are conducting studies involving human subjects and are seeking funding through grant applications.
02
Institutions and organizations that are required to comply with federal regulations regarding human subjects research.
03
Principal investigators and co-investigators who are submitting a Just-in-Time Human Subjects Review Grant Application.
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People Also Ask about

All JIT materials must be submitted via the JIT feature in the eRA Commons or directly to the Grants Management Specialist by an Authorized Business Official. NIH will not accept JIT information submitted by the PI.
To submit a No-Cost Extension: Search for a particular award using the Status - General Search option. Select the Extension action from the three-dot ellipsis menu on the Status Result - General Search screen. The Extension action does not appear if the project period was previously extended by the awarding office.
The JIT feature allows a Signing Official to electronically submit additional grant application information that qualifies for submission and is requested by the grantor agency. The additional information is requested after a peer review of a grant application has been completed and prior to funding.
NIH utilizes a “just-in-time” (JIT) process to collect time-sensitive information that is not included in the application. Any application with an overall impact score below 30 automatically receives an email from NIH requesting JIT information through eRA Commons.
All JIT materials must be submitted via the JIT feature in the eRA Commons or directly to the Grants Management Specialist by an Authorized Business Official. NIH will not accept JIT information submitted by the PI.
Submitting the RPPR All 3 types of NIH RPPRs are submitted through eRA Commons (there is no form available for download). The Annual and Interim RPPR links can be accessed through the Commons Status tab. The Interim RPPR link will appear one day after the project segment end date, but before it has moved to closeout.

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The Just-in-Time Human Subjects Review Grant Application Signature Page is a document required for grant applications that involves research on human subjects. It serves as a certification that the necessary ethical reviews and approvals have been obtained prior to starting the research.
Researchers and institutions that are applying for grants that involve human subjects are required to file the Just-in-Time Human Subjects Review Grant Application Signature Page.
To fill out the Just-in-Time Human Subjects Review Grant Application Signature Page, applicants should provide information such as the research title, principal investigator details, institution information, and certification of necessary approvals from an Institutional Review Board (IRB).
The purpose of the Just-in-Time Human Subjects Review Grant Application Signature Page is to ensure compliance with ethical standards and to confirm that the research protocols involving human subjects have been reviewed and approved by the appropriate ethical review board.
The information that must be reported includes the research title, principal investigator's name and contact information, details of the reviewing IRB, approval status, and signatures from the principal investigator and institutional representatives.
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