Meaningful Use Stage II
There must be a guideline someplace that suggests proposing too much so that you can reduce the proposal after adverse public comment…
Read MoreAuthor: William Hyman
FDA/FCC on Wireless Medical Devices
Posted by William Hyman | Standards & Regulatory |
…concern for the proliferation of devices using radio technology as well as reliance on consumer grade communication devices.
Read MoreProgress (?) on Clinical Decision Support
Posted by William Hyman | Healthcare IT |
“Expert System or One Guy’s Opinion”
Read MoreThe 25 Elements of “Meaningful Use”
Posted by William Hyman | Healthcare IT |
Number 13’s implementing decision support rules is perhaps one of the issues that is closer to the core interests of readers here.
Read MoreFDA Posts New Draft Guidance on Computer-Assisted Detection Devices
Posted by William Hyman | Standards & Regulatory |
While designers of such systems like to say it is “just an aid” and thereby in part try to avoid responsibility for the quality of the output, the likely reality is that it will be relied upon, and therefore a high level of performance should be assured.
Read MoreWhat (if anything) can the recent Sidekick problem teach us?
Posted by William Hyman | Patient Safety |
Let’s always pause long enough to do some risk management thinking…
Read MoreCanada Posts “Medical Device Data System” Rule
Posted by William Hyman | Standards & Regulatory |
Any software that receives and manipulates patient data is a medical device.
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