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BioWorld - Wednesday, May 13, 2026
Home » Authors » Liz Hollis

Liz Hollis

Articles

ARTICLES

Tape measure wrapped around feet on scale

Obesity-focused Allurion scoops up $34M in new funding

Jan. 8, 2020
By Liz Hollis
The obesity problem is one that is affecting a growing number of people globally. With both device and drug companies looking to take on the challenge of combating the problem, Allurion Technologies Inc. has set its sights on advancing a new approach in the U.S. Now, the Natick, Mass.-based company has scored $34 million in new funding through a securities financing and a growth capital term loan. The round was led by Novalis Lifesciences and Romulus Capital, with participation from Ido Investments and ex-Covidien CEO Jose Almeida.
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1-7-lifepod-ihome.png

Experts look to the future of voice tech in health care

Jan. 7, 2020
By Liz Hollis
LAS VEGAS – Over the past three years or so, voice technology has been on the rise, with hospitals looking to leverage it to help patients. Tech companies have taken notice; for example, Amazon assisted with technology to make voice skills HIPAA-compliant, with six skills unveiled as part of that effort.
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BioWorld MedTech’s Cardiology Extra for Jan. 6, 2020

Jan. 6, 2020
By Liz Hollis
Keeping you up to date on recent developments in cardiology.
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Saluda’s closed-loop SCS system continues to see positive results as company awaits word from FDA

Jan. 6, 2020
By Liz Hollis
Saluda Medical Pty. Ltd., of Artarmon, Australia, made waves in 2019, winning the CE mark for its Evoke closed-loop spinal cord stimulation (SCS) system. The good news kept coming following the publication of results from a pivotal study in The Lancet Neurology.
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Health professional touching screen, digital/medical icons

PwC focuses on how digital transformation in health care will impact consumers

Dec. 30, 2019
By Liz Hollis
Will the digital transformation in health care start to benefit consumers in 2020? That was one of the challenges addressed in a recent report from PwC Health Research Institute titled “Top health industry issues of 2020: Will digital start to show an ROI?” The report predicts that in the next year, health system leaders will tout their investments in technology and transformation.
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Bioworld MedTech’s Cardiology Extra for Dec. 30, 2019

Dec. 30, 2019
By Liz Hollis
Keeping you up to date on recent developments in cardiology.
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Medtronic Device: Autoguide Stealthstation

FDA gives nod to Medtronic’s Stealth Autoguide system for cranial procedures

Dec. 18, 2019
By Liz Hollis
Dublin-based Medtronic plc reported Wednesday that the U.S. FDA has given the green light to its Stealth Autoguide system. The company said it is the first cranial robotic platform that integrates with its enabling technology portfolio to create an end-to-end procedural solution.
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Telehealth illustration

Pear Therapeutics, Novartis look to tackle depressive symptoms in MS patients

Dec. 17, 2019
By Liz Hollis
Digital therapeutics have made great strides in recent years, with Pear Therapeutics Inc. playing a key role. Now, the company has reported the dosing of the first patient in part two of a study assessing Pear-006 to address depressive symptoms in multiple sclerosis (MS).
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Telehealth illustration

Pear Therapeutics, Novartis look to tackle depressive symptoms in MS patients

Dec. 17, 2019
By Liz Hollis
Digital therapeutics have made great strides in recent years, with Pear Therapeutics Inc. playing a key role. Now, the company has reported the dosing of the first patient in part two of a study assessing Pear-006 – which Pear Therapeutics is developing in collaboration with Basel, Switzerland-based Novartis AG – to address depressive symptoms in multiple sclerosis (MS).
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bsx-exalt-duodenoscope-hero-12-16.png

Boston Scientific scores FDA win with first single-use duodenoscope

Dec. 16, 2019
By Liz Hollis
Boston Scientific Corp., of Marlborough, Mass., has won the U.S. FDA’s nod for the Exalt Model D single-use duodenoscope for use in endoscopic retrograde cholangiopancreatography (ERCP) procedures. It is the first single-use duodenoscope on the market and earlier secured breakthrough device designation. “Unlike duodenoscopes that are used on multiple patients, a fully disposable duodenoscope doesn’t need to be reprocessed, eliminating the risk of potential infection due to ineffective reprocessing,” said Jeff Shuren, director of the FDA’s Center for Devices and Radiological Health.
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View All Articles by Liz Hollis

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