QIAGEN N.V. today announced its latest initiative to increase global access to advanced cervical cancer screening technologies for women most in need. It includes the commercial launch of QIAGEN’s CE marked careHPV Test and the introduction of a new CE marked self-collection claim for its sampling device, the digene HC2 Collection Device.
The careHPV Test is the first HPV diagnostic specifically designed for regions with limited healthcare infrastructure. As such, the test enables the worldwide implementation and expansion of HPV-based cervical cancer screening, including in areas where women are not screened otherwise. Human papillomavirus or HPV is the primary cause of cervical cancer.
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