Fujirebio Diagnostics

Content by Fujirebio Diagnostics

|2 min read

Fujirebio Receives 510(k) Clearance for Lumipulse® G pTau 217/ β-Amyloid 1–42 Plasma Ratio IVD Test for Alzheimer’s Disease

First blood-based in vitro diagnostic test to receive FDA clearance to help identify patients with amyloid pathology associated with Alzheimer’s disease
|1 min read

Fujirebio Diagnostics Announces Initiation of Clinical Testing for SARS-CoV-2 Antigen Assay

As a leading provider of immunoassays to the diagnostic industry, Fujirebio, as a global team, is joining the fight to combat the COVID-19 pandemic with the goal of providing the first fully automated antigen test
Page 1 of 1