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HRPP Regulations
Office
The Tufts Health Sciences Human Research Protection Program (HRPP) complies with all U.S. regulatory requirements related to the protection of human research participants.
https://viceprovost.tufts.edu/hrpp-regulations
A compilation of resources for IRB researchers.
https://viceprovost.tufts.edu/policies-forms-guides/helpful-links-researchers-hs-irb
Scientific Review Committee
Office
The SRC reviews applicable clinical research proposals to ensure that they meet an acceptable standard of scientific rigor and merit prior to IRB review.
https://viceprovost.tufts.edu/scientific-review-committee
https://viceprovost.tufts.edu/policies-forms-guides/meals-sponsored-awards
COVID-19 Research Cluster
Research Lifecycle
https://viceprovost.tufts.edu/covid-19-research-cluster
Gather, Process & Analyze Data
Research Lifecycle
Tufts provides a variety of tools and resources to ensure efficient and effective strategies that help you get the most out of your data.
https://viceprovost.tufts.edu/gather-process-analyze-data
CTSI Informatics Core
Resource
The CTSI Informatics Core strives to reduce barriers for conducting clinical and translational research for the Tufts community and outside investigators.
https://viceprovost.tufts.edu/research-services/core-facilities-resources/ctsi-informatics-core
IRB authorization agreements (also called Reliance Agreements) are arrangements between two or more institutions that allow IRBs to cede review to one another.
https://viceprovost.tufts.edu/irb-authorizationreliance-agreements