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/Train/chrTrain.asp#citi

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/

 

Community Medical Center IRB Forms (MS Word documents)

 

• Adverse Event Reporting Form

• Area Director Agreement to Participate in Research

• Continuing Review Form

• FDA Guidance on Investigator Responsibilities

• IRB Application

• IRB Exempt Certification Form

• IRB Expedited Review Application

• IRB Incident Form

• IRB Research Study Modification Form

• IRB Study Registration Mnemonic Request Form

• Request for IRB Waiver of Patient Authorization

• Report Form for Emergency Use of Drug or Device

• Research Patient Registration Cover Sheet

• Subjects who do not Read Speak or Understand English