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Biospecimen Repository Services (BRS) Shared Resource Please return completed form to: Diane Shanahan, Program Support Coordinator Email: Hannah cine.Rutgers.edu Tel: 7322353511 Application for Identified
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How to fill out BRS deidentified tissue-data use-IRB:

01
Review the guidelines: Familiarize yourself with the guidelines and requirements for filling out the BRS deidentified tissue-data use-IRB form. It is important to fully understand the purpose and scope of the form before proceeding.
02
Obtain the necessary information: Gather all the relevant information and data that will be required to complete the form accurately. This may include details about the tissue samples, the research project, and any associated participants or collaborators.
03
Complete the form sections: Start by providing your personal information as required, such as name, contact details, and affiliation. Then proceed to fill out the specific sections of the form related to deidentified tissue-data use and IRB (Institutional Review Board) compliance.
04
Provide a detailed description: In the form, provide a comprehensive description of the research project involving the deidentified tissue data. Include information about the purpose, objectives, methods, and expected outcomes of the study. Be clear and concise in your explanation to ensure a better understanding by the reviewing authority.
05
Address ethical considerations: Discuss any ethical considerations related to the use of deidentified tissue data. Explain how participant privacy and confidentiality will be protected, and provide details on any measures taken to minimize any potential risks or benefits associated with the study.
06
Collaborator information: If there are any external collaborators involved in the research project, provide their details and explain their role in the study. This information helps the reviewing authority assess the validity and credibility of the research.

Who needs BRS deidentified tissue-data use-IRB?

01
Researchers conducting studies involving deidentified tissue data: Scientists or researchers who are utilizing deidentified tissue data for their studies need to fill out the BRS deidentified tissue-data use-IRB form. This ensures that the research project adheres to ethical and legal guidelines and protects the rights and privacy of the participants involved.
02
Institutional Review Boards (IRBs): IRBs, which are responsible for reviewing and approving research projects involving human subjects, require researchers to complete the BRS deidentified tissue-data use-IRB form. The purpose is to assess the potential risks, benefits, and ethical considerations associated with the use of deidentified tissue data.
By following these steps and providing accurate information, researchers can properly fill out the BRS deidentified tissue-data use-IRB form and ensure compliance with ethical standards during their research involving deidentified tissue data.
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BRS deidentified tissue-data use-irb refers to the Institutional Review Board approval required for the use of deidentified tissue data in research.
Researchers and institutions conducting research using deidentified tissue data are required to file BRS deidentified tissue-data use-irb.
The BRS deidentified tissue-data use-irb form must be completed with details of the research project, how the deidentified tissue data will be used, and the steps taken to protect participant privacy.
The purpose of BRS deidentified tissue-data use-irb is to ensure that research using deidentified tissue data complies with ethical standards and protects participant confidentiality.
Details about the research project, data use protocols, and measures taken to deidentify tissue data must be reported on BRS deidentified tissue-data use-irb.
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