Sorry, you need to enable JavaScript to visit this website.
Skip to main content
Study

Using FDA reports to inform a classification for health information technology safety problems.

Magrabi F, Ong M-S, Runciman WB, et al. Using FDA reports to inform a classification for health information technology safety problems. J Am Med Inform Assoc. 2012;19(1):45-53. doi:10.1136/amiajnl-2011-000369.

Save
Print
March 21, 2012
Magrabi F, Ong M-S, Runciman WB, et al. J Am Med Inform Assoc. 2012;19(1):45-53.
View more articles from the same authors.

This study reviewed nearly 900,000 reports from the FDA Manufacturer and User Facility Device Experience database (MAUDE) and identified 678 reports describing health information technology issues. Investigators uncovered problems with software functionality, system configuration, interface with devices, and network configuration as new categories to the existing classification system.

Save
Print
Cite
Citation

Magrabi F, Ong M-S, Runciman WB, et al. Using FDA reports to inform a classification for health information technology safety problems. J Am Med Inform Assoc. 2012;19(1):45-53. doi:10.1136/amiajnl-2011-000369.

Related Resources From the Same Author(s)
Related Resources