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BioWorld - Wednesday, April 8, 2026
Home » Topics » North America » U.S.

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Device in heart

Edwards exceeds Wall Street expectations in Q2, in spite of COVID-19

July 24, 2020
By Meg Bryant
Edwards Lifesciences Corp. reported better-than-expected results when it released its second quarter earnings late July 23, with revenue down 15% to $924 million, from $1.1 billion in the same period of 2019. The results beat Wall Street consensus of $797.5 million, and reflected an uptick in surgical procedures that had been delayed by the COVID-19 pandemic. The Irvine, Calif.-based company sustained a net loss of $121.9 million, or $0.20 per share, based on generally accepted accounting principles (GAAP), a sharp drop from $242.3 million, or $0.38 per share, in the same quarter last year. However, adjusted earnings looked brighter at $0.34 per share.
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Electrical activity of the brain
EEGs and endotypes

From cells to cortices, ways to improve neurological disease classification

July 24, 2020
By Anette Breindl
Cancer treatment has been transformed, at its root, by a transformational change in how it is classified. Those successes have not escaped the notice of researchers in other areas of biomedicine, and diseases including heart failure, asthma and polycystic ovarian syndrome are being looked at with an eye to subdividing them in ways that brings diagnostics into the molecular era.
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Telehealth illustration

CBO scoring a significant hurdle in proposals to permanently expand telehealth coverage

July 23, 2020
By Mark McCarty
The support for permanent changes to Medicare coverage of telehealth has risen drastically in the months since the COVID-19 pandemic began, but Krista Drobac of Sirona Strategies said on a July 23 webinar that stakeholders will have to help make the case that telehealth is cost effective. That cost effectiveness argument may be absolutely crucial if any of the related legislative proposals are to stand up to budget scoring in a time of skyrocketing U.S. budget deficits, she said.
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Cybersecurity data lock

Culture of scientific exchange seen as a risk factor for life science cybersecurity

July 22, 2020
By Mark McCarty
The U.S. government has charged two citizens of China with cybercrime in connection with purported hacking of research into vaccines for the SARS-CoV-2 virus, but more than one speaker on a July 22 webinar said scientists involved in basic life science research at universities fail to appreciate the need for cybersecurity, a problem they may take with them to the private sector.
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Da Vinci Xi with operating room staff

Intuitive Surgical beats expectations in Q2 despite COVID-19

July 22, 2020
By Liz Hollis
Robotic-assisted surgery-focused Intuitive Surgical Inc. revealed its second-quarter results late July 21, with worldwide Da Vinci procedures falling about 19% vs. the same period of 2019. Driven by this decline, second quarter 2020 instruments and accessories (I&A) revenue fell by 20% to $461 million, vs. $579 million in the second quarter of 2019.
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COVID-19 vaccine vials behind U.S. capitol building

Pfizer and Biontech to receive $1.95B for first batch of COVID-19 vaccine

July 22, 2020
By Lee Landenberger
The U.S. government will pay $1.95 billion to Pfizer Inc. and Biontech SE for the first 100 million doses of their jointly developed mRNA-based COVID-19 vaccine once Pfizer manufactures it and receives the FDA’s approval or emergency use authorization. The two companies agreed, as part of Operation Warp Speed, to begin delivering 300 million doses of a COVID-19 vaccine in 2021.
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U.S., China wrecking balls

Hacking indictment details decade of thefts, ramps up U.S.-China tensions

July 22, 2020
By Mari Serebrov
The alleged activities of two Chinese hackers outlined in a federal indictment unsealed Tuesday offer “concrete examples of two concerning trends,” U.S. Assistant Attorney General John Demers said, as U.S.-China relations further soured with the news of the charges.
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Speaker at MDIC forum says FDA keen on patient perspectives regarding medical devices

July 21, 2020
By Mark McCarty
The U.S. FDA has put a considerable amount of emphasis on patient perspectives regarding medical devices in recent years, the subject of a recent webinar hosted by the Medical Device Innovation Consortium (MDIC). One of the speakers on the webinar, Carrie Kuehn, of Evidation Health of San Mateo, Calif., said that not only do device makers have a trove of valuable data at their fingertips with patient preference data, but also that the FDA’s message is, “if patients say something, we want to hear about it.”
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Person receiving vaccine

COVID-19 vaccines on track, but is the public ready?

July 21, 2020
By Mari Serebrov
A safe, effective COVID-19 vaccine may be available by the end of the year or early next year, as will the supplies needed to deliver and administer hundreds of millions of doses. That’s the message five biopharma executives delivered to a House subcommittee July 21 as they updated U.S. lawmakers on the progress their companies are making on the vaccine front.
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Digital illustration of U.S., coronavirus

Trautman: COVID-19 may hamper FDA’s efforts to further harmonize Part 820, ISO 13485

July 17, 2020
By Mark McCarty
The U.S. FDA’s interest in harmonizing its regulations for medical devices with an international standard is a matter of record, but the agency has found this to be an enormously complicated task. Kim Trautman, executive vice president for medical device services at NSF International, of Ann Arbor, Mich., told BioWorld that the task of rewriting Part 820 to meet ISO 13485 in the middle is no mean feat, but also that it may be delayed again, this time because of the COVID-19 pandemic.
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