Author: Jeremy Wood
Date: 02-11-03 06:58
IRBtool helps researchers figure out how the common rule and FDA IRB regulations apply to their research. The tool covers exempt/expedited/full review, vulnerable populations, and consent/assent/permission.
You can try the tool at www.irbtool.com
The tool is designed to be educational, as well as useful.
Researchers, IRB members, and staff can use it.
IRBtool will be most useful where it is tailored to reflect an institution’s particular policies and integrated with the institution’s work processes (so that researchers will use it and so that it will deliver them to the appropriate IRB forms).
The tool is easy to customize. The tool’s developer can work with institutions on customizations, or users can license the tool and tailor it themselves.
--Jeremy
jeremy@irbtool.com
610 389 2757
|
|
