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https://viceprovost.tufts.edu/policies-forms-guides/how-submit-single-irb-studythrough-eirb
https://viceprovost.tufts.edu/policies-forms-guides/guidance-course-completion-and-training-data-standard
https://viceprovost.tufts.edu/policies-forms-guides/chemical-resistant-glove-guide
https://viceprovost.tufts.edu/policies-forms-guides/hs-irb-stem-cell-research-policy
https://viceprovost.tufts.edu/policies-forms-guides/onboarding-slides-hs-irb
https://viceprovost.tufts.edu/policies-forms-guides/concoa-cga-connection-reference-chart
The IRB will review direct advertisements (per FDA guidance, “advertising that is intended to be seen or heard by prospective subjects to solicit their participation in a study”) for each research
https://viceprovost.tufts.edu/policies-forms-guides/direct-advertising-material-recruitment
https://viceprovost.tufts.edu/policies-forms-guides/tips-being-prepared-inspection-audit
https://viceprovost.tufts.edu/policies-forms-guides/guidance-requirements-modification-exempt-human-subjects-research