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Subcontract P.I.’s Responsibilities for
INBRE Reporting and Annual Assessment
July 16, 2004 The IDeA Networks of
Biomedical Research Excellence (INBRE) Grant was awarded to the state of
Idaho by the National Institutes of Health (NIH) and the National Center
for Research Resources (NCRR). One condition of the INBRE grant is the
submission of a very detailed annual progress report to NIH and NCRR.
The extensive information required by NIH and NCRR for the annual
progress report is all encompassing and requires specific information,
ranging from individual participants to campus wide data from all
participating institutions. In order to complete the annual progress
report to NIH/NCRR, we will require each institution to submit a
detailed annual progress report to the administrative INBRE office at
the University of Idaho. Below you will find a list of questions you
may expect to see on the annual progress report for your
institution.
While reviewing the information below,
please keep in mind:
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Although the
information we are requesting may seem extensive, please know
that we are only requesting the information that NIH requires us
to provide in the annual progress report. NIH uses this
information to justify the National INBRE Program to the U.S.
Congress.
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The information
requested is for one project period/budget period or one year of
the grant usually from May 1st – April 30th.
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As the subproject P.I. you are
responsible for coordinating all assessment data related to
INBRE funded research. This includes disseminating reporting
information and assuring all INBRE funded researchers (faculty,
students, and staff) submit required information timely,
accurately, and in the requested format.
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Expect to see a request for this information sometime between
October and December each year.
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All data will be submitted on-line through the INBRE on-line
assessment database.
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Please keep in mind that all information listed below is subject
to change. The examples below are based on the information
NIH has requested us to report in the past. It is possible
that NIH may choose to change the information they require us to
report. Should NIH change the information they require from us,
we will alter questions we ask of you accordingly.
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The information provided below is
only an example. Detailed reporting requirements,
definitions, and instructions will be provided at annual
assessment time. |
Example of Institutional Data Required
for Annual Progress Report to NIH/NCRR
(All data is for one project
period/budget period)
Other information:
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Be aware that you must provide
documentation for all Human Subjects and Animal Use. You must submit
all documentation to the INBRE office. Even if you are exempt….we need
an exemption letter from your IRB. Failure to obtain written
pre-approval for all research involving Human Subjects or Animal Use
will result in non-reimbursement of those expenses. This includes
pre-approval on any new protocols or changes in animal use mid project.
This is a requirement of NIH. Even if you have approval through
another agency you must be re-approved through NIH.
·
Notify us immediately
regarding changes in staffing.
Definition of terms:
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*Junior Investigator is (1) an
individual who does not have or has not previously had an external,
peer-reviewed Research Project Grant (RPG) or Program Project Grant
(PPG) from either a Federal or non-Federal source that names that
investigator as the PI or (2) an established investigator who is making
a significant change to his/her career.
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*Independent Status - the PI and
External Advisory Committee (EAC) can determine that a junior
investigator has achieved independent status either by receipt of an RPG
or PPG and/or through an indication that independence has been achieved
through the acquisition of sufficient skills and knowledge.
·
*Research Project Grants (RPG)
and Program Project Grants (PPG) include the following: RPGs: R01, R34,
R35, R37, R41, R42, R43, R44, U01, U19, U43, U44 PPGs: P01, P42.
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