New! 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.
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