AstraBio is proud to announce that its plasma Phosphorylated tau-217 (p-tau217) Immune Test Kit has officially received Class II medical device registration approval
2025-02
Suzhou AstraBio Technology Co. Ltd help to get Science articles published
2025-01
Astrabio, a global innovator in neurobiomarker detection, was honored to participate as a special guest at the signing ceremony of the Memorandum of Understanding between Eisai (Thailand) Marketing Co., Ltd.and Bangkok Genomics Innovation PLC.
2024-09
Suzhou AstraBio Technology Co. Ltd has helped to complete a study on the diagnostic performance of four plasma biomarkers (GFAP, α-syn, NfL, p-tau181) in FTD patients based on a single-molecule immunoassay technology.
2024-08
Suzhou AstraBio Technology Co. Ltd has successfully obtained NMPA for two single-molecule-based blood test kits: GFAP Protein Assay and NFL Protein Assay.
2024-05
Suzhou AstraBio Technology Co. Ltd completed tens of millions of yuan Pre-B+ round of financing, the future of immunoassay technology high-end brand as the goal, to accelerate the AD early screening and early diagnosis market layout.
2024-03
Suzhou AstraBio Technology Co. Ltd has completed tens of millions of yuan of Pre-B round of financing, will be the core of the neurological markers, to further improve the neurological blood markers screening and diagnostic solutions.
2024-02
AD blood reagents kit based on single-molecule analysis strategy successfully receives NMPA approved:
β Amyloid 1-42 reagents kit
Phosphorylated tau 181 reagents kit
2023-08
ASTRABIO passed the ISO 13485:2016 medical device quality management system certification.
2022-11
The fully automated single-molecule immunoassay analyzer AST-DxSMD developed by ASTRABIO has now under registration for application as an innovative medical device.
2022-06
ASTRABIO completed nearly 100 million CNY Series A financing to create a closed-loop industrial chain for clinical transformation of novel biomarkers.
2022-06
Our first fully automated fluorescence immunoassay analyzer based on single-molecule analysis strategy approved as Class II medical device.