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BioWorld - Tuesday, December 23, 2025
Home » Topics » U.S., BioWorld MedTech

U.S., BioWorld MedTech
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Coronavirus vs U.S. wrecking balls

Harvard’s Mina says ‘archaic view’ of testing impeding cheap surveillance testing for COVID-19

Aug. 7, 2020
By Mark McCarty
The COVID-19 pandemic has sparked some innovation in testing, but not all that innovation has made it to market. Michael Mina, an assistant professor of epidemiology at the Chan School of Public Health at Harvard University, said on an Aug. 7 conference call that the U.S. FDA’s “archaic view” of testing is impeding the use of paper strip tests he said would turn the tide in the effort to contain the pandemic.
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Health professional pointing stethoscope at Clinical Trial words, icons

Aronson says validated outcome measures are desperately needed for clinical evidence

Aug. 6, 2020
By Mark McCarty
Real-world evidence (RWE) and clinical trial data might seem to bear little resemblance to each other, but Naomi Aronson, executive director for clinical evaluation at the Blue Cross and Blue Shield Association, said there are problems common to both. The most significant of these is an absence of validated outcomes measures for many conditions, measures Aronson said are “desperately” needed in order to make an appropriate coverage determination.
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U.S. FDA headquarters

Saliva-based tests for COVID-19 continue to perplex FDA, test developers

Aug. 5, 2020
By Mark McCarty
Developers of tests for the SARS-CoV-2 virus have gained a tremendous amount of experience in a very small amount of time, and of all the media for sampling, saliva offers the easiest route for test administration. The U.S. FDA’s Tim Stenzel said on the Aug. 5 testing town hall, however, that the FDA and developers have discovered that this is an extremely difficult medium to work with.
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Physician with patient

Saykara mobile AI assistant improves practice productivity 500%

Aug. 5, 2020
By Annette Boyle
Saykara Inc.’s artificial intelligence (AI) assistant enabled the Midwest Institute for Minimally Invasive Therapies (MIMIT Health) to boost practice productivity five-fold. The voice-enabled iOS-based app, named Kara, drafts visit summaries, updates the electronic health record, produces prescriptions, and more with limited involvement from clinicians.
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Coronavirus and stock charts

Despite fall in net sales, Zimmer Biomet beats consensus in Q2

Aug. 4, 2020
By Liz Hollis
Orthopedic companies felt pressure from COVID-19 in their most recent quarters. For example, Zimmer Biomet Holdings Inc. reported second-quarter net sales of $1.226 billion, a decrease of 38.3% from the prior-year period. Still, those revenues did come ahead of expectations, as Wells Fargo analyst Larry Biegelsen noted – $432 million ahead of his group's estimate and $305 million ahead of consensus.
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U.S. White House

White House moves on telehealth executive order to counter rural hospital closure

Aug. 4, 2020
By Mark McCarty
The Trump administration has issued an executive order designed to improve access to telehealth for Medicare beneficiaries in rural America, making permanent numerous changes that had been temporarily added for the COVID-19 pandemic. The news arrives as the Centers for Medicare and Medicaid Services (CMS) posted the draft Medicare physician fee schedule (MPFS) complete with expanded use of telehealth for a number of services.
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Artificial intelligence and digital health icons

Investor unruffled over FDA’s approach to AI in discussion paper

Aug. 3, 2020
By Mark McCarty
A number of entities have sounded off on the FDA’s discussion paper for artificial intelligence (AI), including several medical societies that would like to see autonomously operating algorithms subjected to more stringent review than supervised algorithms. Vibhor Rastogi, general partner at Symphony AI of Los Altos, Calif., told BioWorld that the company is on board with many of these concerns, adding that the FDA discussion paper does a “good job of balancing innovation and patient safety.”
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Product image

Setpoint to start U.S. pivotal trial for RA implant around year end

July 31, 2020
By Stacy Lawrence
A bioelectronic platform that stimulates the vagus nerve to reduce inflammatory activity and restore balance in the immune system is the ultimate aim of Setpoint Medical Inc. The Valencia, Calif.-based startup is preparing to start a U.S. pivotal trial for its most advanced program in rheumatoid arthritis (RA) later this year or early next.
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U.S. NIAID Director Anthony Fauci

Fauci ‘cautiously optimistic’ about a vaccine for COVID-19, says scientific values not compromised

July 31, 2020
By Mark McCarty
The issue of the U.S. federal government’s response to the COVID-19 pandemic was revisited yet again in a hearing in the House of Representatives. While partisanship was on full display, Anthony Fauci, director of the National Institute of Allergy and Infectious Diseases, said he is “cautiously optimistic” about the prospects for a vaccine and that the development of candidates has not compromised scientific principles.
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Personal protective equipment (PPE)

Transparency of both supply and demand for PPE seen as critical in Senate hearing

July 30, 2020
By Mark McCarty
The U.S. Senate Finance Committee met for a second time in three days to address the supply of personal protective equipment (PPE) for the COVID-19 pandemic. While a witness said the Defense Production Act (DPA) is no panacea for production, one message emerging from the hearing is that producers need to hear from end users about demand just as much as users need to know about available inventories.
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