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The US FDA Has Approved Roche's New Streamlined Workflow Process
Jun 27, 2013The US Food and Drug Administration (FDA) has approved Roche's new streamlined workflow process for the cobas Human Papillomavirus (HPV) Test, which help labs reduce costs, improve turnaround time and focus on other key tasks. Roche ...
Tags: Cobas HPV Test, FDA Approval, Medicine
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Guided Therapeutic Obtains CE Mark Approval for Non-Invasive Luviva Advanced Cervical Scan
Jul 19, 2012Guided Therapeutics has obtained CE mark approval for its non-invasive LuViva advanced cervical scan. The approval is based on a US multi-center, pivotal trial, which enrolled 1,607 women at risk for developing cervical disease, to detect ...
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