Clarification
of Protection of Human Subjects Test Requirement
It is also important to note that persons obtaining
informed consent should be included in this section of the summary safeguard
statement. In many cases, the IRB will accept completion of another university's
human subjects test requirement for those investigators from other academic
institutions, so be sure to note at which institutions collaborators will
be performing aspects of the research. Any research submitted to an IUPUI/Clarian
IRB is subject to this requirement.
Additional
IRB Requirements for VA-Funded Studies Involving Human Subjects
Previously, the requirement applied to only NIH-funded
studies. Section 3 requests information regarding the race and gender of study
participants. In addition, the IRB must receive one copy of the grant proposal
for each new study submitted to the IRB involving VA funding. IRB Continuing
Review Forms will be updated on the Research Compliance Web site to reflect
this change.
Routing
of Electronic Proposals
Electronic proposals continue to be under the same
guidelines as paper proposals and must receive institutional review and approval
prior to submission to the funding agency.
Electronic submissions take various forms including
preparation of the proposal directly on an agency's web site or the electronic
transmission of files. In all cases, the appropriate number of paper copies
for internal use should be routed through the department, dean's office, and
Research and Sponsored Programs (R&SP) with a Route Sheet. Once approved,
R&SP will either submit the proposal electronically or notify the project
director to proceed with the electronic submission. Contact R&SP for instructions
or guidance.
|
|
Research and Sponsored
Programs
UN 618
General - 274-8285
Research Compliance - 274-8289
Sponsored Program Development - 278-0249
|
|
|
|
Please send comments,
requests to subscribe or unsubscribe, to RSPCOMMU@iupui.edu.
|
