Connected Health Document Health Data HIPAA 
Health Populi
FEBRUARY 8, 2021
Accelerate digital health. Secure health data (updating privacy/HIPAA). The Manatt document is a wonderful example of a company’s clear articulation of values and corporate social responsibility in an era of declining trust between citizens and institutions, found in the 2021 Edelman Trust Barometer.
Health Populi
MARCH 10, 2020
Department of Health and Human Services unveiled the long-anticipated ONC Cures Act Final Rule for health data interoperability. That’s a wonky phrase that translates, simply put, into how our health data will be made available to us patients, consumers, health plan members, caregivers all.
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Health Populi
MARCH 2, 2021
The coronavirus pandemic accelerated digital transformation of organizations, including health care providers. Consumers’ trust in all sources of health information increased between 2018 and 2020 except for peoples’ trust in online health websites/apps and social media, both of which lost a number of consumers trusting them.
Health Populi
NOVEMBER 12, 2019
“Google’s ‘Project Nightingale’ Gathers Personal Health Data on Millions of Americans,” the Wall Street Journal reported in today’s paper and on the WSJ.com website. ” Here’s Ascension’s press release on the collaboration , described in the title as “healthcare transformation.”
Enzyme Health
JUNE 19, 2019
CCHP: CCHP stands for the Center for Connected Health Policy and is a non-profit that has been designated the national telehealth policy resource center. CMS is the federal agency that administers HIPAA standards and develops Medicaid and Medicare reimbursement policies for telemedicine.
Healthcare IT News - Telehealth
MAY 6, 2020
In an age when nearly everyone is digitally connected in some way – even many senior citizens, who are often characterized as technophobic – it only makes sense that the healthcare industry is seeing a lot of connected health devices and remote patient monitoring (RPM) technologies.
Health Populi
JULY 1, 2019
Not only that, they directed the streams of data to researchers who were standing by, catching every drop, like phlebotomists filling vial after vial. This data would not go to waste and patients had a forum to act on their own desires to carefully document and share their experiences for the benefit of themselves and others.
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