Roche granted FDA Breakthrough Device Designation
Roche announces that the Tina-quant lipoprotein Lp(a) RxDx assay receives Breakthrough Device Designation from the FDA
Source: selectscience.net
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Roche granted FDA Breakthrough Device Designation for blood test measuring Lp(a) – a key marker for hereditary cardiovascular risk
Approximately one in five people worldwide have elevated Lp levels, putting them at increased risk of cardiovascular diseases including myocardial infarction and stroke.1The Roche Diagnostics...
Source: marketscreener.com
F. Hoffmann-La Roche Ltd: Roche granted FDA Breakthrough Device Designation for blood test measuring Lp(a) - a key marker for hereditary cardiovascular risk
Approximately one in five people worldwide have elevated Lp(a) levels, putting them at increased risk of cardiovascular diseases including myocardial infarction and stroke.1The Roche Diagnostics Tina-quant®
Source: finanznachrichten.de
FDA Approves Self-Collection cobas HPV Test for Early Detection of Cervical Cancer Early
In 2014, the cobas human papillomavirus test was approved by the FDA for first-line, primary screening in women aged 25 years and older.
Source: pharmacytimes.com
Roche gains FDA approval of HPV self-collection solution
Expanding access and screening options to help eliminate cervical cancer
Source: selectscience.net