UCI Investigators are required to use the UCI IRB approved (UCI seal in
footer) version of the consent form when obtaining signed informed
consent (unless the IRB has granted a waiver or alteration of the
consent process).
To ensure that your research team is using the most current version of
the IRB approved consent form, always download your approved consent
documents from the e-Doc Depot http://apps.research.uci.edu/irbdocs/ ,
upon receiving email notification that the submission (i.e., continuing
protocol application, modification or new study application) has been
approved by the IRB. Also be sure to download the current UCI IRB
approval letter.
The requirements for UCI IRB approval (e.g., informed consent process
and HIPAA Research Authorization) are noted on the letter. Prior to
obtaining informed consent double check the approval and expiration
dates listed in the footer of the IRB-approved consent – the date of
consent must be within the IRB approval period. For more information
about the requirements for informed consent at UCI, please refer to the
Human Research Protections Policies and Procedures
http://www.research.uci.edu/ora/hrpp/hrppPolicies.htm .
OR-IRB-HRP mailing list
OR-IRB-HRP@department-lists.uci.edu
http://department-lists.uci.edu/mailman/listinfo/or-irb-hrp
