Response Biomedical Cleared for Rapid Respiratory Syncytial Virus Test
Response Biomedical Corp announces that it received a US FDA 510(k) clearance to market a rapid Respiratory Syncytial Virus (RSV) test.
Read MoreResponse Biomedical Corp announces that it received a US FDA 510(k) clearance to market a rapid Respiratory Syncytial Virus (RSV) test.
Read MoreDxS Ltd announces it is working closely with AstraZeneca to make available a companion diagnostic for use with IRESSA (gefitinib), AstraZenecas treatment for non small cell lung cancer (NSCLC).
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