Library Search Results

 Library Search Results

Results from your Search are visible below.  You may further refine your search using the Refine Your Results links below, right.  Clicking on one of the refinement items will return a subset of your original search.  To return to your original results, simply choose the "Any [term] link at the top of each section.  You may also sort your results, either by Relevance/Ranking (default result), Title, or Date Modified. 
1-10 of 68 results
Sort by: 
UAB Procedure
This procedure outlines the responsibilities of the Investigator, OIRB and IRB regarding the informed consent process and documentation of informed consent.
UAB Policy
These guidelines outline UAB's approach for charging tuition remission and other graduate student compensation for students who work on and are supported by institutional or sponsored projects.
UAB Procedure
This procedure outlines the responsibilities of the OIRB and the IRB for documentation of convened IRB proceedings.
UAB Procedure
This procedure outlines the responsibilities of the investigator, OIRB and IRB for approving a waiver or alteration of the consent process and the waiver of consent documentation.
UAB Procedure
This procedure outlines the responsibilities of the Investigator, IRB, and OIRB for handling Investigator and Institutional Conflicts of Interest.
UAB Procedure
This procedure outlines the responsibilities of the investigator, OIRB and IRB with regard to suspension or termination of IRB-Approved research and administrative hold.
UAB Procedure
This procedure outlines the responsibilities of the investigator, OIRB and IRB for continuing review of research approved by the convened IRB.
UAB Procedure
This procedure lists responsibilities of the investigator, ORIB and IRB for communication among IRBs.
UAB Procedure
This procedure describes how human materials or data not involving human subjects may be classified as Not Human Subjects Research.
UAB Procedure
This procedure lists responsibilities of the investigator, IRB, OIRB, and sponsor for waiver to the informed consent process in research planned for emergency settings.