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BioWorld - Friday, March 20, 2026
Home » Topics » Medical technology, Regulatory

Medical technology, Regulatory
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Aussie device makers urge TGA to follow IMDRF lead on software regulations

Nov. 13, 2019
By Mark McCarty
Australia's Therapeutic Goods Administration (TGA) recently posted a draft guidance for regulation of software as a medical device, but the Medical Technology Association of Australia expressed a preference for an international standard for risk classification.
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Regulatory front for Nov. 13, 2019

Nov. 13, 2019
The latest global regulatory news, changes and updates affecting medical devices and technologies.
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hologic-3Dquorum-11-13.png

Following solid quarterly results, Hologic gains FDA nod for 3Dquorum imaging tech

Nov. 13, 2019
By Liz Hollis
Marlborough, Mass.-based Hologic Inc. got good news from the U.S. FDA, which has given the green light for the 3Dquorum imaging technology, which employs Genius AI. The technology works along with Hologic's Clarity HD high-resolution imaging technology to reduce tomosynthesis image volume for radiologists by 66%, the company said.
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DNA

FDA clears first whole exome sequencing platform for overall tumor mutation burden

Nov. 13, 2019
By Meg Bryant
Nanthealth Inc. has received U.S. FDA clearance for a whole exome sequencing test to determine overall tumor mutational burden (TMB) in cancer tissue. Known as Omics Core, the first-of-its-kind in vitro diagnostic test is available now as part of Nanthealth's GPS Cancer molecular profiling suite.
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Regulatory front for Nov. 12, 2019

Nov. 12, 2019
The latest global regulatory news, changes and updates affecting medical devices and technologies.
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Regulatory front for Nov. 11, 2019

Nov. 11, 2019
The latest global regulatory news, changes and updates affecting medical devices and technologies.
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Latest telehealth bill would dismantle some geographic restrictions

Nov. 11, 2019
By Mark McCarty
Advocates of telehealth are backing the bipartisan, bicameral Connect for Health Act of 2019, which would eliminate geographic and origination site restrictions on Medicare coverage and save billions of taxpayer dollars.
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FDA sign

People problems cited as the root of most duodenoscope issues

Nov. 8, 2019
By Mark McCarty
The U.S. FDA's two-day advisory hearing on industrial ethylene oxide (EtO) sterilization of medical devices wrapped up with a discussion of how duodenoscopes can be made safer. The conclusion was largely that employee churn, training and work conditions were the biggest challenges – issues over which the FDA has nearly zero leverage.
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FDA panel says tweaks are the best short-term answer to EtO controversy

Nov. 7, 2019
By Mark McCarty
The first day of the FDA's two-day hearing on ethylene oxide (EtO) sterilization of medical devices addressed several alternatives to EtO, but the advisory panel had little advice to offer the agency other than to encourage tweaks to sterilization procedures in order to get past the immediate problem.
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Nevro aims to dominate SCS with first system to deliver all frequencies

Nov. 7, 2019
By Stacy Lawrence
The U.S. FDA has approved the Senza Omnia Spinal Cord Stimulation (SCS) system from Redwood City, Calif.-based Nevro Corp. The system is the first such system that delivers Nevro's high frequency 10,000 Hz stimulation, known as HF10, but also all other therapeutic spinal cord stimulation frequencies.
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