FDA clears Meridian TRU Legionella test
TRU Legionella provides optimized detection of Legionella pneumophila serogroup 1 that is most commonly associated with Legionnaire’s disease. TRU Legionella allows the laboratories with a cost effective and
The US Food and Drug Administration (FDA) has granted priority review to Roche’s supplemental biologics licence application (sBLA) for Gazyva/Gazyvaro (obinutuzumab) to treat adults with primary membranous nephropathy (pMN).