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INSTITUTIONAL REVIEW BOARD INFORMATION
All UCSF Faculty, Fellows, Residents, Medical Students and Key Research Personnel must complete mandatory training in the protection of human subjects in research through the Collaborative Institutional Training Initiative. Information regarding this UCSF requirement can be found at:
http://www.research.ucsf.edu/chr/Recruit/chrCFformats.asp
To complete the training, go to www.citiprogram.org
Create a login & password, then choose UCSF as the affiliated institution.
Please call the IRB Office at 499-6553 for any questions.
UCSF: http://www.research.ucsf.edu/CHR/
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Starting March 27, 2017 the CMC IRB Office will accept submissions electronically through CyberIRB. If you have any questions regarding CyberIRB, please do not hesitate to contact our office at 499-6552 or IRB@communitymedical.org If this is your first time logging into the website, please contact the IRB Office at 559-499-6552 so our office can send you a username and temporary password. |
1. FDA Guidance Investigator Responsibilities 2. Study Proposal Format 3. Study Participant Information Sheet Template |
For assistance with all aspects of obtaining IRB approval for your research, and for assistance in submitting your materials to the IRB, please email IRB@communitymedical.org or call the IRB office at 559-499-6553. Our office is located in the second floor of the UCSF Fresno Building, Room 290.