Shape the future of cervical cancer screening.
Identify HPV 31
BD ONCLARITY™ HPV ASSAY IS THE ONLY FDA AND HEALTH CANADA APPROVED HPV TEST THAT INDIVIDUALLY IDENTIFIES HPV 31.
HPV 31 POSES A HIGHER RISK FOR CERVICAL PRECANCER AS COMPARED TO HPV 18.
The BD Onclarity™ HPV Assay with extended genotyping allows for a more precise, accurate way to measure a woman’s risk for developing cervical pre-cancer and cancer compared to an assay with partial genotyping.1,2,3 HPV 31 identification matters. Extended genotyping is critical.
Learn more about extended genotyping with the BD Onclarity™ HPV Assay
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Extended genotyping allows for a more precise way to measure your patient’s risk for developing cervical pre-cancer and cancer vs. a pooled, high-risk assay.
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Shape the future of cervical cancer screening with BD Onclarity™ HPV Assay
* ASCCP, American Society for Colposcopy and Cervical Pathology; CIN, Cervical Intraepithelial Neoplasia; HPV, human papillomavirus
1. Monsonego J et al. Gynecol Oncol. 2015;137(1):47-54.
2. Stoler MH et al. Am J Clin Pathol. 2019;151(4):433-42.
3. Salazar K et al. J Am Soc Cytopath. 2019;8:284-92.
4. Perkins RB et al. J Low Genit Tract Dis. 2020;24:102-31.
5. Bonde JH et al. J Low Genit Tract Dis. 2020;24(1):1-13.
6. Drolet M et al. Lancet. 2019;394(10197):497-509.
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