Einstein's New FWA Number: Einstein has a new FWA Number: 00023382. For more info see our FAQs.
The IRB has new staff: Check our staff list to see an updated contact list.
Informed Consent Documents have been updated: Updated consent documents are available here and in the iRIS help menu.
Epic is here: Learn more about required language in consent documents.
Documentation of Human Subjects Education for NIH-funded Studies: Learn more about creating these documents for NIH-funded studies.
Migration of "pre-iRIS" studies to iRIS is complete: Learn more about how to complete the process.
Required Clinical Research GCP Certification: Learn more about the new requirement for GCP training that applies to all key personnel involved in the conduct of new and ongoing drug and device studies which took effect January 1, 2015.
iRIS is now required for all new study submissions (Exempt, Expedited, and Full Board)! Learn more, visit the iRIS Info Page, review the Frequently Asked Questions (FAQ), and register for an optional training session.
The Einstein Human Research Protection Program (HRPP) promotes and protects the rights and welfare of all human research participants. Affiliated organizations include all of the colleges and schools of Yeshiva University, Montefiore Medical Center, Jacobi Medical Center and North Central Bronx Hospital.
Einstein's two IRBs* (formerly known as the Committee on Clinical Investigations (CCI) and the Montefiore Medical Center IRB) facilitate excellence in human research by extending personalized guidance and support to the research community through timely and high quality service, education, review, and monitoring. Two IRB meetings are held monthly to review full board items while all other transactions are reviewed upon receipt on an ongoing basis.
*An Institutional Review Board is a committee, operating under Federal regulations, State laws, and institutional policy, that reviews research involving human subjects to ensure the ethical and equitable treatment of those subjects.