Regulatory Knowledge and Support
Specific Aims
Aim 1. Streamline the scientific and regulatory review process for
clinical research protocols and merge the common Web-based ARIA interface with
the TRI Portal.The TRI will integrate numerous review bodies across
multiple campuses and establish uniform review criteria for clinical research
protocols. This innovative, integrated organizational structure for research
support services will be accessible to all investigators through the Web-based
interface and to TRI researchers via the TRI Portal.
Aim 2. Improve the knowledge of the research community with regard
to ethical study design, data management, human subject protection, and
regulatory guidelines. Provision
of exemplary training for investigators, research staff, and members of
institutional review committees is critical to the development of an effective
research organization. Specific and individualized training will be offered
through the Research Support Center (RSC) for investigators and coordinators who
are new to research.
Aim 3. Increase the availability and
optimize the utilization of exceptional human research advocacy resources. We propose to assist TRI investigators by ensuring
that research compliance guidelines are maintained at the highest standards.

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