FCC: New 5G framework fosters health IT innovation
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The FCC's 5G rules could enable health IT innovations such as remote medical care, mobile applications and wireless body sensors, according to a top agency official.
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The Federal Communications Commission voted to adopt a flexible framework to make wireless spectrum bands above 24 GHz available for 5G commercial use, and the White House announced a $400 million research plan led by the National Science Foundation that builds on the vote.
5G isn't a particular system or standard. It's more of a catchall term for what will replace the existing 4G state-of-the-art wireless, carrier-based connectivity.
Julius Knapp, chief of the FCC's Office of Engineering and Technology, said one of the most significant outcomes of the new rules could be the advancement of health IT capabilities.
"We don't know exactly what 5G is, but we do know it will provide high-speed, high-capacity, low-latency wireless networks," he said at a Brookings Institution event on July 19.
The new framework and the high-speed wireless network it expands could furnish "the incentive to drive competition and bring new services to the [health IT] market," Knapp said.
"All sorts of novel health care applications have been developed" or are in development, he added. He cited the use of wireless medical devices, body sensors and telemetry to help doctors treat patients without in-person interaction.
Additionally, Knapp said the commission's plans "open a world of possibilities" for the future of health care, and the increased speed afforded by 5G technology could enable physicians to perform surgery remotely, detect health issues early through wearable devices and communicate with remote patients in real time.
"The Internet of Things...is fundamentally about the ability to connect with anything or anyone at anytime," he said.
However, the increase in connectivity comes with "the need to build cybersecurity protections into the standards," Knapp added.
He said the FCC is engaged in "constant dialogue" with the Food and Drug Administration, the agency charged with developing cybersecurity guidance for medical devices.
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