healthcare
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Fax Technology is the Cornerstone of Interoperability. Here's Why.
Fax is the dominant information exchange technology in U.S. healthcare, outpacing secure direct messaging 25-to-1. Most of that is exchanged using inefficient and unsecure machines. With the emergence of cloud-based fax technology to facilitate secure system-to-system document transfer, the use of cloud fax needs to be part of every CTO's/CIO's digital strategy...The evolution of fax from paper-based to cloud transmission and storage - Cloud Fax Technology (CFT) - is a key step that enables providers to comply with HIPAA and other regulations. Further strengthening CFT as a key component in Healthcare Information Systems (HIS) is its evolution into Direct Messaging platforms, enabling the seamless exchange of Patient Health Information (PHI) between the diverse data and document management systems used by labs, pharmacies, doctor's offices, hospitals, and billing providers. CFT supports and contributes to the goal of interoperability...
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FCC To Fund $400M Yearly For Rural Telehealth Networks
The Federal Communications Commission will make $400 million available annually to healthcare providers to expand the development of broadband telehealth networks from a pilot to a permanent program. Read More »
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FCC To Hire Healthcare Director, Step Up Health Efforts
The Federal Communications Commission (FCC) held a public briefing this week with its mHealth Task Force, which formed just this past June to work with various other healthcare professionals and technologists to create a report full of “concrete” next steps that the FCC (and other agencies) can take to facilitate the adoption and acceleration of mHealth in the United States. Read More »
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FCC to Look into Possible Problems Using Wireless Medical Devices
Studies show that mobile medical devices, such as the ability to recieve dialysis at home for kidney disease patients, could save as much as $197 billion over the next 25 years while improving patient care. Read More »
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FDA Antimicrobial Resistance Guidelines Fail to Address Root Causes
Last December, the Food and Drug Administration (FDA) published two controversial documents on its website: Guidance 213 and the Veterinary Feed Directive (VFD). The guidelines stirred a firestorm of protests from public health offiicials who argue that the guidelines are too weak to prevent the continuing growth of antibiotic resistant germs...the crisis, as outlined by Dr. Joseph Mercola, is that we are now "facing the perfect storm to take us back to the pre-antibiotic age, when some of the most important advances in modern medicine – intensive care, organ transplants, care for premature babies, surgeries and even treatment for many common bacterial infections – will no longer be possible." Read More »
FDA Approves Home Health Platform
Federal regulators have approved Verizon's first foray into the home monitoring space. Read More »
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FDA Clears IND For First Clinical Trial Protocol Developed Using Crowdsourcing
Transparency Life Sciences, LLC (TLS), the world's first drug development company based on open innovation, today announced that its Investigational New Drug Application (IND) to assess lisinopril as an adjunctive therapy for multiple sclerosis (MS) has been cleared by the US Food and Drug Administration (FDA). Read More »
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FDA Fails To Protect Against Antibiotic Resistance, Guarantees More Needless Death And Suffering
Antibiotic-resistant bacteria infect two million Americans every year, causing at least 23,000 deaths. Even more die from complications related to the infections, and the numbers are steadily growing. Read More »
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FDA Guidance On Medical Device Cybersecurity: Too Little Too Late?
The Food and Drug Administration (FDA) has taken an important step forward in better protecting patients and their data with the release of new guidelines on managing cybersecurity risks of medical devices this week. Despite being a step in the right direction, it unfortunately comes late...
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FDA Lays Out Rules For Some Smartphone Health Apps
Food and Drug Administration officials say they will begin regulating a new wave of applications and gadgets that work with smartphones to take medical readings and help users monitor their health. Read More »
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FDA Offers Guide On Wireless Healthcare Devices
The Food and Drug Administration has published a guide to the use of wireless healthcare devices in healthcare settings. Read More »
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FDA Scrutinizes Antibacterial Products For Hormonal Disruption, Bacterial Resistance
[...] The FDA has announced that it is formally reconsidering “antibacterial” soaps and other personal-care products, charging that the antibacterial ingredients confer no benefit over regular soap and water while carrying extra risks. Read More »
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FDA Takes Significant Steps To Address Antimicrobial Resistance
The U.S. Food and Drug Administration today is implementing a plan to help phase out the use of medically important antimicrobials in food animals for food production purposes, such as to enhance growth or improve feed efficiency. The plan would also phase in veterinary oversight of the remaining appropriate therapeutic uses of such drugs. Read More »
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FDA Wants To Leverage Electronic Medical Records To Probe For Adverse Events
Keeping track of adverse events is a tricky task, even for regulators. Even when a drug has undergone a rigorous premarket assessment process, some risks may not become evident until a product is used by millions. And for other drugs, a particularly rare but serious side effect may take months, if not years, to be identified. Read More »
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Federal Cuts Threaten Healthcare System For Alaska Natives
The 10-year federal “sequestration” plan of steady cuts could devastate the healthcare system that Alaska Natives rely on, speakers at a conference of tribal leaders said Wednesday. Read More »
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