... after all, a full Electronic Medical Record/Order Entry/Decision Support system is far more complex, with potential for far more immediate patient impact, then pharma's research IT systems.
Yet the former is unregulated.
PhRMA , you should start lobbying to create your own private Certification Commission For Pharmaceutical IT (CCPIT) now.
You can start certifying all your IT by going through a checklist of features, and avoid those pesky FDA inspections just as hospital do!...
Those Goddamn Plaintiff's Trial Lawyers Are to Blame...
It seems the EHR pundits are starting to notice one of the side effects of EHR technology: the liabilities EHRs impose on users.Of course, such liabilities are presented as the fault not of a...
Science or Politics? The New England Journal on "The...
In the NEJM article "The Meaningful Use Regulation for Electronic Health Records", David Blumenthal, M.D., M.P.P. (ONC Chair) and Marilyn Tavenner, R.N., M.H.A. (10.1056/NEJMp1006114, July...
Is H. Stephen Lieber, CEO of HIT Industry Trade Group...
In the Wall Street Journal article today entitled "Can Technology Cure Health Care?" by erstwhile WSJ reporter Jacob Goldstein, H. Stephen Lieber, CEO of the health IT trade group HIMSS...
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