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This document serves as an addendum to the IRB application for studies using CTRC facilities and services. It outlines the necessary components and requirements for submitting a study proposal.
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How to fill out clinical and translational research

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How to fill out Clinical and Translational Research Center Addendum

01
Begin by reviewing the guidelines provided by the Clinical and Translational Research Center (CTRC).
02
Gather necessary documentation related to your research project, such as protocols and consent forms.
03
Fill out the addendum form, ensuring all required fields are completed accurately.
04
Include detailed descriptions of the research objectives, methodologies, and any special considerations.
05
Review your entries for clarity and completeness.
06
Submit the addendum to the appropriate administrative office for review.
07
Follow up on the submission status and address any feedback or additional requirements from the CTRC.

Who needs Clinical and Translational Research Center Addendum?

01
Researchers conducting clinical trials or translational research requiring support from the Clinical and Translational Research Center.
02
Investigators seeking access to specialized resources, facilities, or expertise provided by the CTRC.
03
Anyone part of a collaborative research project that involves clinical and translational methodologies.
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The Clinical and Translational Research Center Addendum is a supplementary document required for research proposals that outlines specific details regarding the clinical and translational aspects of the study, such as methodologies, objectives, and compliance with regulatory requirements.
Investigators and research teams conducting clinical and translational research within the Clinical and Translational Research Center framework are required to file the Clinical and Translational Research Center Addendum.
To fill out the Clinical and Translational Research Center Addendum, researchers should provide detailed information on the research objectives, methodologies, participant recruitment strategies, ethical considerations, and data management plans. It is essential to follow the provided guidelines and templates.
The purpose of the Clinical and Translational Research Center Addendum is to ensure that research proposals meet the necessary requirements for clinical and translational research, facilitate review processes, and enhance collaboration between researchers and clinical entities.
The Clinical and Translational Research Center Addendum must report information including study objectives, design, recruitment methods, ethical considerations, potential risks, data management processes, and compliance with legal and regulatory requirements.
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