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diagnostics

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  • Australian regulators approve Atomo’s rapid HIV diagnostic kit
    • News

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  • Australian regulators approve Atomo’s rapid HIV diagnostic kit
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  • Australian regulators approve Atomo’s rapid HIV diagnostic kit
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  • Australian regulators approve Atomo’s rapid HIV diagnostic kit
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Latest Articles

  • Atomo Locks in US$410K Pascal Order as FebriDx Demand Accelerates in the US
    Atomo Locks in US$410K Pascal Order as FebriDx Demand Accelerates in the US
    • News

  • PainChek locks in performance data for FDA submission, aiming to be  first pain assessment app approved in US
    PainChek locks in performance data for FDA submission, aiming to be first pain assessment app approved in US
    • News

  • HeraMED eyes TGA reclassification to restore HeraBEAT device for at-home use
    HeraMED eyes TGA reclassification to restore HeraBEAT device for at-home use
    • News

  • dorsaVi secures $110k in contracts across mining, healthcare, and shipping sectors
    dorsaVi secures $110k in contracts across mining, healthcare, and shipping sectors
    • News

  • Compumedic hits record medtech diagnostics revenue with growth in US and China being targeted
    Compumedic hits record medtech diagnostics revenue with growth in US and China being targeted
    • News

  • Australian regulators approve Atomo’s rapid HIV diagnostic kit
    • News

    Australian regulators approve Atomo’s rapid HIV diagnostic kit

    Medtech company Atomo Diagnostics (ASX: AT1) has been granted regulatory approval in Australia for their patented AtomoRapid HIV (1&2) rapid diagnostic kit which will enable testing for HIV with just one drop of blood. The approval granted by the Therapeutic Goods Association (TAG) enables Atomo to commence distribution of the diagnostic test to medical professionals

    Read More
    Public
  • FDA approves Imugene to commence human trial for lung cancer immunotherapy
    • News

    FDA approves Imugene to commence human trial for lung cancer immunotherapy

    Biopharma company Imugene (ASX: IMU) is now on their way towards commercialisation of their lung cancer treatment with approval from the US Food and Drug Administration (FDA) to commence human trials. With the project name PD1-Vaxx in the US, the approval enables Imugene to commence recruiting patients for a clinical trial of the treatment on

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    Public
  • Telix submits FDA application for new prostate cancer imaging product
    • News

    Telix submits FDA application for new prostate cancer imaging product

    It may soon be easier for prostate cancer to be diagnosed at an early stage with Telix Pharmaceuticals (ASX: TLX) having submitted their radiopharmaceutical imaging technology to the Food and Drug Administration for approval. The New Drug Application (NDA) comes after completing clinical trials across more than 600 patients which builds on peer-reviewed clinical research

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    Public
  • ASX IPO April: Atomo Diagnostics Limited
    • News

    ASX IPO April: Atomo Diagnostics Limited

    With only one company set to list this month, it appears that the volatility that surrounds the ASX is prompting some companies to delay listing until some degree of normality in financial markets is restored.  One company brave enough to face the current environment is Atomo Diagnostics Limited (Proposed ASX: AT1). The Sydney-based medical diagnostics

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    Public
  • AdAlta partners with GE Healthcare to develop i-body diagnostic imaging
    • News

    AdAlta partners with GE Healthcare to develop i-body diagnostic imaging

    Melbourne-based drug development company AdAlta (ASX: 1AD) has been selected by GE Healthcare, one of the world’s largest healthcare companies, to develop ‘i-bodies’ which GE can use as imaging agents.  One-tenth of the size of regular antibodies, i-bodies are a new class of human protein therapeutic which can be applied as a therapeutic drug to

    Read More
    Public
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