What if I told you that there was a plant that could be used to treat diabetes, liver problems, ulcers, leukemia, and malaria? Understandably, you would want that plant to be studied and turned into ...

Institutional Biosafety Committee – recombinant DNA, materials of human or non-human primate origin, toxins, select agents, etc. Radiation Safety Committee – radioactive materials Institutional Review ...

The flowchart and steps below outlines the best practice for processing industry-written and sponsored clinical trials at UAB. There are many small steps in each of the larger defined steps (see flow ...

Follow the step-by-step instructions below to successfully maintain and close a protocol with the IRB. Instructions below include information about continuing reviews, amendments, event reporting (new ...

If the information collected by your project is to be kept in house (i.e. not to be shared with the public) or collected for pedagogical reasons,( i.e., teaching purposes), it is not considered ...

A single IRB (sIRB) of record will be used in the ethical review of non-exempt human subjects research protocols funded by federal agencies that are carried out at more than one site in the United ...

The Post Approval Monitoring (PAM) team within Research Regulatory Affairs aims to help ensure the well-being of humans and vertebrate animals involved in research. Authorization for researchers to ...

The following steps were used to achieve the objectives: Central Support: A central PSPO office was established with minimal required staffing for provision of support to clinicians for protocol ...

The Institutional Review Board (IRB) will now utilize the online submission platform, Research Enterprise Solutions (RES), for NEW human subjects research applications. New IRB studies will no longer ...

The Quiet Knee protocol, which some HSS surgeons began implementing several years ago, takes a more conservative approach to knee replacement recovery than traditional clinical protocols. This new ...