FDA clearance of the BD Onclarity Self-Collection Kit in April 2026 enables at-home HPV testing for cervical cancer screening, expanding access and addressing barriers for under-screened populations.
New automated workflow combines at-home sampling with robotic lab processing.
BD's HPV Assay has been added to the ASCCP Risk-Based Management Guidelines, leveraging extended genotyping for enhanced HPV screening.
A first-of-its-kind HPV self-collection pilot program has launched in Texas to improve cervical cancer screening access in underserved areas.
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Labcorp’s adoption of artificial intelligence technology aims to enhance the screening process for cervical cancer.
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A new study reveals that 85% of women would welcome the option to choose between self-sampling and nurse-led HPV cervical screening.
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In this episode of Clinical Lab Chat, we discuss what sample self-collection means for the diagnosis and treatment of HPV and cervical cancer.
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BD is shipping its FDA-approved HPV self-collection kits to healthcare facilities, offering an accessible cervical cancer screening option.
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A new study has identified specific biomarkers in cervical mucus that could improve accuracy in the early detection of cervical cancer.
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Seegene demonstrated its new HPV diagnostic products and emphasized the importance of HPV screening at the AOGIN conference.
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Researchers developed a urine test using ELISA to detect HPV16 E7 oncoproteins, a noninvasive method for cervical cancer screening.
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A new study highlights support among healthcare providers for HPV self-collection, which could improve access to cervical cancer screening.
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Researchers developed an effective cervical cancer screening method, which detects more cancers and precancerous stages than current methods.
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BD received FDA approval for women to self-collect vaginal specimens for HPV testing, expanding access to cervical cancer screening.
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che received FDA approval for its HPV self-collection solution, allowing individuals to collect their own samples.
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An at-home cervical cancer screening device received Breakthrough Device status to help increase testing access for people in need.
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Researchers developed a urine-based test utilizing whole genome sequencing to detect DNA fragments released by head and neck tumors.
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The research highlighted factors influencing cervical cancer screening and highlighted the need for interventions to increase screening.
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