Daily Journal Staff Writer
SAN DIEGO - Health care providers that modernize electronic systems for managing patient information could be exposed to additional liability under a new rule issued this year by the U.S. Food and Drug Administration.
The rule, issued for the regulation of medical device data systems, is supposed to smooth the approval process for device manufacturers. One unintended side effect is that hospitals and...
To continue reading, please subscribe.
For only $95 a month (the price of 2 article purchases)
Receive unlimited article access and full access to our archives,
Daily Appellate Report, award winning columns, and our
Verdicts and Settlements.
Or
$795 for an entire year!
For only $95 a month (the price of 2 article purchases)
Receive unlimited article access and full access to our archives,
Daily Appellate Report, award winning columns, and our
Verdicts and Settlements.
Or
$795 for an entire year!
Or access this article for $45
(Purchase provides 7-day access to this article. Printing, posting or downloading is not allowed.)
Already a subscriber?
Sign In