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Get the free Single IRB for Multi-Site or Cooperative Researchgrants.nih.govSS11/13 - Internal Ra...

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IRB Approved From: 09/20/2012 To: 11/13/2012UNIVERSITY OF PENNSYLVANIA HEALTH SYSTEM Gilead Sciences, Inc. GSUS2160130, Amendment 1, 5OCT2011 A Phase 3b, Open label, Single Arm Study to Evaluate the
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How to fill out single irb for multi-site

01
Determine if your study qualifies for single IRB review for multi-site.
02
Obtain approval from the local IRB of the lead site.
03
Identify the participating sites and obtain their agreement to rely on the single IRB.
04
Ensure all sites have the necessary documentation and training for the single IRB review process.
05
Fill out the single IRB application form accurately and completely, ensuring all required information is provided.
06
Submit the completed application to the single IRB for review and approval.

Who needs single irb for multi-site?

01
Researchers conducting multi-site studies involving human subjects.
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Single IRB for multi-site is a single Institutional Review Board (IRB) that reviews and oversees a research study conducted at multiple sites.
Researchers conducting a multi-site study are required to file a single IRB for multi-site.
To fill out a single IRB for multi-site, researchers must provide all relevant information about the study protocol, study sites, and any potential risks or benefits to participants.
The purpose of a single IRB for multi-site is to streamline the IRB review process, reduce administrative burden, and enhance research participant protections in multi-site studies.
On a single IRB for multi-site, researchers must report the study protocol, informed consent documents, recruitment materials, and any adverse events or protocol deviations.
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