The Northwestern University IRB Office is primarily responsible for developing and directing the University’s Human Subject Protection Program (HSPP).
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IRB - Institutional Review Board | Northwestern University | irb-staging.nubic.northwestern.edu Reviews
https://irb-staging.nubic.northwestern.edu
The Northwestern University IRB Office is primarily responsible for developing and directing the University’s Human Subject Protection Program (HSPP).
irb-staging.nubic.northwestern.edu
Training and Education | Institutional Review Board (IRB), Northwestern University
http://irb-staging.nubic.northwestern.edu/training
Northwestern University - Office for Research. FWA, IORG and Registration Letter. Become an IRB Member. Templates, Forms and SOPs. Information for Panel Members. Northwestern University requires all individuals involved in the conduct of human subjects research to complete initial human subjects protection training. And to recertify every 3 years. IRB approval will be withheld if these training requirements have not been met. Principal Investigators and Co-investigators,. PDF) that must be met. This file...
Which Type of Review? | Institutional Review Board (IRB), Northwestern University
http://irb-staging.nubic.northwestern.edu/process/new-study/reviews
Northwestern University - Office for Research. FWA, IORG and Registration Letter. Become an IRB Member. Templates, Forms and SOPs. Information for Panel Members. Which Type of Review? Research involving human subjects must comply with the regulations set forth by the U.S. Department of Health and Human Services (HHS) at 45 CFR 46 and the Food and Drug Administration at 21 CFR 50 and 56. Not Human Subjects Research Submissions. Human Subjects Research Submissions. Once the application is submitted by the ...
Submission Process | Institutional Review Board (IRB), Northwestern University
http://irb-staging.nubic.northwestern.edu/process
Northwestern University - Office for Research. FWA, IORG and Registration Letter. Become an IRB Member. Templates, Forms and SOPs. Information for Panel Members. The IRB has gathered the following information to assist with protocol submissions. If you have a question that is not answered in these pages, please contact the IRB office directly: irb@northwestern.edu. Or (312) 503-9338 on the Chicago campus or (847) 467-1723 in Evanston. Arthur Rubloff Building, 7th Floor. 750 N Lake Shore Dr.
Submission Requirements | Institutional Review Board (IRB), Northwestern University
http://irb-staging.nubic.northwestern.edu/process/new-study/requirements
Northwestern University - Office for Research. FWA, IORG and Registration Letter. Become an IRB Member. Templates, Forms and SOPs. Information for Panel Members. Determine who will serve as the Principal Investigator. Every research study requires a Principal Investigator (PI). This person takes full responsibility for the conduct of the study. Below is a comprehensive list of who may and may not serve as PI. Non-tenure-track research and/or clinical faculty (full, associate, and assistant professors);.
Panel Meetings | Institutional Review Board (IRB), Northwestern University
http://irb-staging.nubic.northwestern.edu/panels
Northwestern University - Office for Research. FWA, IORG and Registration Letter. Become an IRB Member. Templates, Forms and SOPs. Information for Panel Members. Northwestern University has established multiple IRB panels to review research:. IRB Panels A, B, C, and D review biomedical new studies, revisions and safety/other events. Reviews biomedical studies that are up for continuing review as well as time sensitive submissions. IRB Panel E reviews social behavioral research. Jesse Brown VA Studies.
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IRB - Institutional Review Board | Northwestern University
Northwestern University - Office for Research. FWA, IORG and Registration Letter. Become an IRB Member. Templates, Forms and SOPs. Information for Panel Members. Continuing Review / Closure. Which Type of Review? Recruitment Materials and Guidelines. Additional Committee Review and Approval. Filling out the eIRB Application. Preparing a modification in eIRB. Investigator's Brochure Changes. Preparing the Continuing Review in eIRB. Preparing the NRI in eIRB. Reporting Requirements and Timeframes.
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