NHSCSP

From April 2015, the DYSIS Colposcope has been recognised as an approved advanced technology by the NHS Cervical Screening Programme (NHSCSP) in the latest UK National Colposcopy Guidelines (Document 20).

The new release of the Document 20 guidelines advises on the latest advancements in cervical screening, and recognises the DYSIS Colposcope for its financial and clinical advantages. The guidelines particularly detail those benefits afforded by the technology relevant to other changes such as the introduction of HPV testing.

The guidelines can be read here.

NICE

In 2010 the UK Regulator, NICE (National Institute of Health and Care Excellence) launched an investigation into the clinical efficacy and cost efficiency of various new technologies in the cervical screening category. The review involved an independent analysis of the published clinical trials followed by a detailed review of the health economics. DYSIS was the only technology deemed to be both clinically effective and cost saving. The report, containing the recommendation from NICE, was published in 2012. The full report can be found by clicking here.

FDA

In 2011 the Food and Drugs Administration in the US granted DYSIS clearance to market. FDA determined that DYSIS with Pseudo-Color imaging (PCI, or DYSISmap) is a digital colposcope designed to image the cervix and lower genital tract under illumination and magnification. Colposcopy is indicated for women with an abnormal Pap smear in order to affirm or detect abnormal appearances consistent with neoplasia, often with directed biopsy. The PCI feature is an adjunctive tool for displaying areas of aceto-whitening. It is a tool that should not be used as a substitute for a thorough colposcopic evaluation.

CE

DYSIS is CE marked and complies with the European Medical Device Directive. DYSIS Medical Ltd. has ISO13485 certification for the quality management system used to design, manufacture and commercialise the DYSIS Colposcope.