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SMART IRB Agreement AddendumPurpose: (1) to highlight the flexible provisions of the SMART IRB Agreement, and (2) to document which options institutions will implement as part of the Ceded Review.
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How to fill out smart irb agreement implementation

01
Read and understand the SMART IRB agreement
02
Gather all necessary information and documents required for the agreement
03
Download the SMART IRB Agreement Implementation document
04
Review the document thoroughly before filling it out
05
Fill out the agreement by providing accurate and complete information
06
Ensure all required signatures are obtained
07
Submit the filled-out agreement to the appropriate authority or organization
08
Follow any additional instructions or steps provided to complete the implementation process

Who needs smart irb agreement implementation?

01
Researchers conducting collaborative studies across multiple institutions
02
Institutional Review Boards (IRBs) responsible for overseeing research activities
03
Organizations or institutions involved in multi-site research projects
04
Researchers wishing to streamline the review process for study protocols

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Smart IRB agreement implementation refers to a streamlined process for the review and oversight of human subjects research across multiple institutions. It allows institutions to rely on a single IRB (Institutional Review Board) for the ethical review of research protocols.
Researchers and institutions that conduct human subjects research involving multiple sites or collaborating institutions are required to file smart IRB agreement implementation.
To fill out the smart IRB agreement implementation, institutions must complete the Smart IRB reliance agreement form, providing necessary information about the study, participating institutions, and the designated IRB responsible for review.
The purpose of smart IRB agreement implementation is to facilitate efficient and consistent ethical review processes, reduce redundancy in the IRB review for multi-site studies, and enhance collaboration among institutions.
Information that must be reported includes the study title, participating institutions, lead investigator details, and specific consent processes, along with data security and privacy considerations.
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