Diagnostics: Page 23


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    Quidel expects COVID-19 test demand to continue through Q2, but offers no 2022 guidance

    CEO Doug Bryant told investors Thursday that Quidel is seeing testing demand moderate in February, but the first quarter will result in the largest revenue in the company's history. The company did not provide full-year guidance.

    By Feb. 18, 2022
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    EU issues guidance on high-risk IVDs, surveillance of legacy medical devices

    The documents outline how notified bodies can meet In Vitro Diagnostic Medical Devices Regulation requirements to verify product batches of high-risk class D diagnostics, and manufacturer rules on quality management systems.

    By Feb. 17, 2022
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    Trendline

    Medical device industry continues to turn to AI

    While the industry continues to embrace artificial intelligence, there are still questions about how the new technologies need to be regulated and if they are effective.

    By MedTech Dive staff
  • Illumina continues to battle EU regulators over premature $8B Grail buy

    CEO Francis deSouza told MedTech Dive that Illumina continues a two-front defense in the European Union — in the courts and with regulators — over its early acquisition of the cancer diagnostics test maker. 

    By Feb. 16, 2022
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    Diagnostics M&A expected to be strong in 2022 after dealmaking took off last year

    Respondents to KPMG's survey predict that deal volumes and values for the diagnostics space will jump again this year as companies are ready to spend more of their COVID-19 cash.

    By Feb. 16, 2022
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    Courtesy of Quest Diagnostics
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    Labcorp, Quest warn COVID-19 testing demand will plummet in 2022

    The rival lab giants told investors during their latest earnings calls that they expect coronavirus-related test volumes to nose-dive by as much as 75%.

    By Feb. 11, 2022
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    Ascension inks strategic relationship with Labcorp, expanding testing capabilities

    Under the terms of the deal, Labcorp will manage Ascension's hospital-based laboratories in 10 states, and acquire select assets of the St. Louis-based system's outreach laboratory business.

    By Rebecca Pifer • Feb. 10, 2022
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    Sarah Silbiger via Getty Images
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    BioCardia, Cook Medical land FDA breakthrough nods in latest designations

    Cardiovascular devices feature prominently in the tech granted regulatory privileges, including a drug-eluting stent for patients with chronic limb-threatening ischemia and a non-invasive cardiac monitoring device. 

    By Feb. 9, 2022
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    Courtesy of Guardant Health

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    Q&A

    Guardant Health targets colorectal cancer screening in 2022

    CEO Helmy Eltoukhy tells MedTech Dive the precision oncology company plans to launch a liquid biopsy in the first half of the year, rivaling Exact Sciences' Cologuard stool test.

    By Feb. 8, 2022
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    Sarah Silbiger via Getty Images
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    Roche partner recalls illegally imported rapid COVID-19 tests from US

    FDA said there are "confirmed reports" of unlawful importation of the Standard Q COVID-19 Ag Home Test and South Korea's SD Biosensor is looking into which distributors or people were involved.

    By Feb. 7, 2022
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    Sarah Silbiger via Getty Images
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    CDRH targets hiring, novel approvals among 2022-2025 strategic priorities

    FDA's Center for Devices and Radiological Health, whose staff continues to struggle with an unprecedented workload since the pandemic's start, is aiming to achieve at least 90% of its annual hiring targets for certain years.

    By Feb. 4, 2022
  • BD Veritor system for rapid detection of SARS-CoV-2
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    Courtesy of BD/PRNewswire
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    BD's Q1 revenue beats Street despite COVID-19 testing decline

    In spite of the pandemic and macroeconomic challenges, CEO Tom Polen said the company has "confidence" to raise 2022 revenue guidance "while remaining appropriately prudent, given the current uncertain environment." 

    By Feb. 3, 2022
  • Thermo Fisher, Hologic plan for extended test demand in 2022

    In a year of ups and downs for COVID-19 testing, both companies are raising revenue guidance for 2022 as the need for diagnostics isn't fading.

    By Feb. 3, 2022
  • Siemens Healthineers CLINITEST rapid COVID-19 antigen test
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    Courtesy of Siemens Healthineers
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    Siemens Healthineers ups 2022 forecast after COVID-19 test boom, but sees increased competition

    CFO Jochen Schmitz told investors Thursday that as competition in the diagnostics space heats up this year, the company expects "revenues to decline sharply in the second half."

    By Feb. 3, 2022
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    Sarah Silbiger via Getty Images
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    Breakthrough device program 'far exceeding' FDA expectations after record year

    The total number of products granted the agency's regulatory privileges in 2021 increased by more than 50%, while the number of novel devices that came to market fell compared to 2020.

    By Feb. 1, 2022
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    Deep Dive

    3 key FDA topics for medtechs in 2022

    While the agency is looking to get back to normal operations this year, COVID-19 is poised to remain a top priority and, once again, thin resources for more traditional work, such as product reviews.

    By , Feb. 1, 2022
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    Roundup: Latest earnings show medtechs grappling with healthcare staffing shortages, supply chain

    Medical device companies ended 2021 on an "uninspiring" note, J.P. Morgan analysts said, as they brace for a slowdown in procedures driven by a surge in COVID-19 cases due to the omicron variant.

    By Jan. 31, 2022
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    iHealth Lab gets DoD order for additional 104M home COVID-19 tests

    The transaction brings the total number of kits the Department of Defense has ordered from iHealth Lab to more than 350 million, putting the company at the heart of the Biden administration's effort to boost testing capacity.

    By Jan. 31, 2022
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    Courtesy of Abbott
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    Abbott Q4 revenue beats estimates on demand for COVID-19 tests; company warns of 2022 uncertainty

    Abbott provided an initial coronavirus test sales forecast of $2.5 billion, which is expected to occur early in the year and will be updated quarterly. Evercore ISI analysts said the company's "testing assumptions seem derisked."

    By Jan. 26, 2022
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    Sarah Silbiger via Getty Images
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    FDA finalizes two guidances on including patient perspectives in medtech clinical trials

    The documents, which elaborate on how to engage patients to improve trial design and use patient-reported outcomes, are based on feedback from groups like AdvaMed which raised concerns about "significant" legal issues.

    By Jan. 26, 2022
  • GE Healthcare's revenue hit by continued supply chain challenges

    GE CEO Larry Culp said Tuesday that ongoing supply chain disruptions were "most acute" in healthcare and will last through at least the first half of 2022, describing the persistent problem as the worst in decades.

    By Jan. 25, 2022
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    Medtech earnings season shows bumpy end to 2021 for some, bonanza for others

    Procedure-dependent companies were negatively impacted to a greater or lesser degree by the surge in omicron cases in their most recent quarters, while COVID-19 test makers benefitted from the spike in demand.

    By Jan. 24, 2022
  • Philips targets Q4 2022 end to recall as supply chain issues drag down results

    The recall, which now impacts 5.2 million sleep apnea and ventilator machines, contributed to a 10% fall in comparable sales in the fourth quarter of 2021, while the increase in affected devices led Philips to up its field action provision.

    By Jan. 24, 2022
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    Permission granted by Roy Mendiola
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    Diagnostics makers ride omicron surge in COVID-19 test demand. But for how long in 2022?

    The highly transmissible variant caused the Biden administration to announce plans to buy 1 billion rapid tests to provide free to Americans. However, when testing will ramp back down remains an open question.  

    By Jan. 20, 2022
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    Dollar Photo Club
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    Exact Sciences posts positive data on Cologuard 2.0 ahead of readouts on rival tests

    A study found Exact's second-generation stool test has a lower false positive rate than the current product and is better at detecting precancerous lesions. But it is facing competing blood tests from Freenome and Guardant Health.

    By Jan. 20, 2022
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    Sarah Silbiger via Getty Images
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    FDA misses MDUFA V deadline after months of contentious talks

    The agency has failed to send the final MDUFA V user fee agreement to Congress by the Jan. 15 deadline, suggesting there may be unresolved disagreements with industry over elements of the program.

    By Jan. 19, 2022