CE marked Real-time PCR for the detection and characterization of the genotypes of Human Papilloma Virus encompassing high risk (16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, 68) and low risk (6, 11, 42, 61 and 70) groups in seven ready to use mastermixes which each include an internal control. The assay is compatible with a wide number of Extraction systems and real-time PCR platforms.