Search
3241 - 3250 of 3310 Results
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