Human
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General information
The website provides resources for the research community in preparing and submitting research protocols and consent forms in compliance with federal regulations and University policies. University Guidelines, federal
regulations, checklists and
templates are provided to
assist the investigator in the proper design and conduct of a protocol
involving human subjects. The site also includes IRB
review fees and the forms required
to submit a protocol application, report a change in the study, obtain
continuing review, report adverse experiences or events and report
the closure of a study. The site will be periodically updated as we revise forms and provide helpful links. Please bookmark this page to ensure easy access to the latest HIC news and forms. Any questions or comments regarding this site should be forwarded to Kathleen Uscinski. HIC Staff and MembersHIC I
Sandra L. Alfano, Pharm. D., F.A.S.H.P., C.I.P. HIC II
Maurice J. Mahoney, M.D., J.D., C.I.P.
Suchitra Krishnan-Sarin, Ph.D.
Administrative StaffMaurice J. Mahoney, M.D., J.D., C.I.P. Sandra L. Alfano, Pharm. D.,
F.A.S.H.P., C.I.P. Kathleen Uscinski, M.B.A., C.I.P. Jean Larson, M.B.A. Cathleen Montano, J.D., C.I.P. Tracy Rightmer, J.D. Brandy Howell, C.I.P. Amy Blakeslee, B.S., C.I.P. Katrina Lehmann Blount, Ph.D. Ellen Bedard, M.S., C.I.P. Christine Earley, M.A. Monika Lau, M.Ed. Jennifer Marchitto Angela Oren, J.D. Dawn Pedevillano, B.S. Kimberly Miniter, A.S. Christine Mangler Fee Schedule
Last modified: Wednesday, 03-Jun-2009 16:53:02 EDT (VM) | ||||||||||||||||||||||||||||||||||||||