Diagnostics: Page 52


  • Rivals LabCorp and Quest post improved outlooks despite PAMA woes

    Quest's volume gains exceeded those of rival LabCorp, but came at the expense of its revenues per requisition, which fell 1.2% in the third quarter.

    By Oct. 24, 2019
  • Device to ID obstructions in post-PCI patients wins breakthrough status

    Swiss startup CorFlow Therapeutics created the device to both assess and treat microvascular obstruction in patients after percutaneous coronary intervention.

    By Oct. 24, 2019
  • the FDA Headquarters Explore the Trendlineâž”
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    Sara Silbiger via Getty Images
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    Trendline

    Top 5 stories from MedTech Dive

    From haphazard layoffs at the Food and Drug Administration to the industry’s current IPO environment and tracking FDA-authorized AI devices, here is a collection of top stories from MedTech Dive.

    By MedTech Dive staff
  • J&J reports rising success rate in robotic surgery clinical trial

    The study is assessing diagnostic abilities of the Monarch robotic surgery platform, which Johnson & Johnson gained in the $3.4 billion acquisition of Auris Health.

    By Oct. 24, 2019
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    UpperEdge
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    Medtronic rolls out AI-assisted colonoscopy system in Europe

    The medtech giant expects to introduce the system in the U.S. market in the second half of 2020, a company spokesperson told MedTech Dive.

    By Oct. 21, 2019
  • Abbott 'working through a handful of items' with FDA on FreeStyle Libre 2

    Third-quarter revenue for the medtech came in at $8.08 billion, slightly below Wall Street expectations, but executives praised the growth of key products FreeStyle Libre, MitraClip and Alinity on its earnings call.

    By David Lim • Oct. 16, 2019
  • Ancestry takes on 23andMe, rolls out genetic health test services

    The company will be working with Quest Diagnostics and Illumina to sell the laboratory developed tests. It does not currently have a relationship with LabCorp, according to an executive.

    By David Lim • Oct. 15, 2019
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    Medical software makers get new guidance on MDR, IVDR

    The European Commission's Medical Device Coordination Group aims to clarify which software will be subject to the new regulations, and how those products should be classified and placed on the market.

    By Dana Elfin • Oct. 14, 2019
  • FDA clears first rapid Ebola virus diagnostic

    Risk of flare up remains, but the United Nations called the outbreak responsible for killing 2,100 people over 14 months in the Democratic Republic of the Congo "significantly contained."

    By Oct. 11, 2019
  • CDS software, labels for staplers and breast implants among FDA 2020 guidance priorities

    The annual publication comes days after the White House issued an executive order aimed at limiting agency use of the documents.

    By David Lim • Oct. 11, 2019
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    Jacob Bell
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    Experimental cancer IVD trial guidance finalized

    AdvaMed won many many of the changes it sought during the comment period, including ones related to communication with the FDA.

    By Oct. 10, 2019
  • Fresenius to pay $5.2M to settle Medicare overbilling allegations

    DOJ alleged the company overbilled Medicare for more than seven years by ordering hepatitis B tests for patients it knew to be immune to the virus.

    By Oct. 10, 2019
  • Qiagen taps new CEO, restructures in 'clearly a bad day'

    The company is also suspending next-generation sequencing-related instrument development as it pivots into a 15-year partnership with Illumina to develop in vitro diagnostic kits.

    By David Lim • Oct. 8, 2019
  • Lantheus strikes deal to buy Progenics, sparking investor backlash

    Velan Capital, a big shareholder in Progenics, accused management of selling at a "massive discount" and preventing investors from being heard.

    By Oct. 3, 2019
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    Former Covance CEO out as LabCorp diagnostics chief a month after appointment

    Newly minted diagnostics CEO John Ratliff is departing the company. LabCorp reshuffled two supply chain and managed care execs to fill the void.

    By David Lim • Updated Nov. 7, 2019
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    Jacob Bell / BioPharma Dive
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    FDA designates AI software meant to boost ultrasound accessibility a breakthrough device

    Led by Livongo and 23andMe veteran Andy Page, newly rebranded Caption Health anticipates pivotal data on its tech will be published in early 2020."

    By Maria Rachal • Oct. 1, 2019
  • DOJ charges 35 people in $2.1B Medicare genetic testing fraud scheme

    CMS also announced it took adverse administrative action against CGx testing companies and providers who filed more than $1.7 billion in claims to Medicare.

    By David Lim • Sept. 30, 2019
  • AI just as effective as docs in medical imaging, study suggests

    Still, researchers cautioned that the data is sparse and warned against sweeping conclusions, noting "the narrow public body of work comparing AI to human physicians."

    By Rebecca Pifer • Sept. 25, 2019
  • EU changes for IVDs called a 'sea change,' revolutionary

    The new in vitro diagnostic regulation, slated to come into effect May 2022, will for the first time subject as many as 90% of these diagnostics to review. Previously, most companies could self-certify.

    By Dana Elfin • Sept. 23, 2019
  • Medtechs keep shareholders happy, potentially at pipeline's expense: EY

    The industry recorded its highest revenues ever within the last year, an analysis by the consultancy shows. Even as R&D spending grew 11%, those investments fell short of the proportion of cash returned to investors.

    By Maria Rachal • Sept. 23, 2019
  • FDA lowers Cologuard age to 45, adding 19M to Exact's screening market

    The labeling change, which some analysts say represents a more than $3 billion annual revenue opportunity, brings Exact Sciences' flagship product in line with updated screening guidelines for colorectal cancer.

    By Maria Rachal • Sept. 23, 2019
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    Amgen Inc.
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    Adaptive lands deal to provide NGS-based cancer tests to Amgen

    The giant biotech will pay annual development fees, sequencing payments and regulatory milestones that could amount to a notable source of revenue for Adaptive.

    By Sept. 19, 2019
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    Quest didn't steal Cedars-Sinai blood test in trade secrets row, jury says

    Hospitals are increasingly using intellectual property to spur transition of early-stage discoveries into products that can be commercialized through licensing agreements.

    By Dana Elfin • Sept. 16, 2019
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    Nurses, physician assistants rarely interpret diagnostic images, study finds

    Researchers at Emory University said the analysis suggests a need for standardized, focused training programs for non-physician professionals to formally define their roles.

    By Sept. 16, 2019
  • Abbott says AI technology can help diagnose heart attacks

    A study in the journal Circulation concluded the algorithm, which aims to individualize testing by taking into account factors such as patient age and sex, performed better than the European Society of Cardiology rule-out pathway.

    By Sept. 11, 2019
  • FDA finalizes guidance on HDEs after AdvaMed scrutiny

    Industry advocates had criticized FDA's tight parameters on which humanitarian use devices are eligible to turn a profit, but the final guidance largely mirrors the draft.

    By Sept. 6, 2019