Health Blawg
JANUARY 16, 2019
HIPAA, everyone’s favorite scapegoat for all (OK, most) of the ills of the modern healthcare-industrial complex, is perpetually called out as being in dire need of a rewrite. The HIPAA RFI came next. A digression: As the health wonks and policy nerds reading this are already aware, HIPAA is a horse of a different color.
Health Blawg
JANUARY 16, 2019
HIPAA, everyone’s favorite scapegoat for all (OK, most) of the ills of the modern healthcare-industrial complex, is perpetually called out as being in dire need of a rewrite. The HIPAA RFI came next. A digression: As the health wonks and policy nerds reading this are already aware, HIPAA is a horse of a different color.
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Health Blawg
DECEMBER 26, 2017
These publications come as part of the FDA’s effort to improve its approach to digital health, to continue to work on drawing the line between digital health tools that are properly regulated as “devices” by the FDA and those that are not. signals from in vitro diagnostic devices.
Medicine and Technology
AUGUST 13, 2013
The Summit will feature: A summary of recent and upcoming policy and regulatory changes that are strengthening patients' rights and ability to access their health data electronically, including Meaningful Use and HITECH modifications to HIPAA.
Health Blawg
DECEMBER 26, 2017
These publications come as part of the FDA’s effort to improve its approach to digital health, to continue to work on drawing the line between digital health tools that are properly regulated as “devices” by the FDA and those that are not. signals from in vitro diagnostic devices.
Health Blawg
DECEMBER 26, 2017
These publications come as part of the FDA’s effort to improve its approach to digital health, to continue to work on drawing the line between digital health tools that are properly regulated as “devices” by the FDA and those that are not. signals from in vitro diagnostic devices.
Health Blawg
DECEMBER 26, 2017
These publications come as part of the FDA’s effort to improve its approach to digital health, to continue to work on drawing the line between digital health tools that are properly regulated as “devices” by the FDA and those that are not. signals from in vitro diagnostic devices.
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