Fujirebio today announced that the U.S. Food and Drug Administration (FDA) has granted 510(k) clearance for the company’s Lumipulse® G pTau 217/β-Amyloid 1-42 Plasma Ratio in-vitro diagnostic (IVD) ...
A research group in Japan identified a correlation between damp heat test of 1,000 hours to 3–6 years of field exposure in humid areas and changes in acetic acid concentration in photovoltaic modules.