Pandemic Control Industry - Diagnostics

Home / Pandemic Control
Company Product R&D / Approval Status
Medigen Vaccine Biologics 80 minutes nucleic acid testing kit (RT-qPCR) TW EUA; EU CE certification; US EUA notified
GeneReach Biotechnology Corp POCKIT™ Central SARS-CoV-2 (orf 1ab) Premix Reagent TW EUA; EU CE certification
LabTurbo Biotech LabTurbo AIO RNA Detection Kit, LabTurbo AIO Viral DNA/RNA Extraction Kit, and LabTurbo AIO SP-qPCR System TW EUA
Kim Forest Enterprise KimForest SARS-CoV-2 Detection Kits EU CE certification; US EUA Approved
TBG Diagnostics ExProbe SARS-CoV-2 Testing Kit EU CE certification; US EUA notified
GeneOne Diagnostics COVID-19 Nucleic Acid Diagnostic Kit EU CE certification; US EUA notified
Applied BioCode BioCode® SARS CoV-2 Assay US EUA notified
PlexBio IntelliPlex SARS-CoV-2 Detection Kit EU CE certification
Quark Biosciences DigiChip SARS-CoV-2 Assay Work with Shin Kong Memorial Hospital and a California-based medical group for clinical validation and to apply for regularly approval.
Industrial Technology Research Institute (ITRI) 60 minutes Nucleic Acid Molecule Detection System
TCI Gene QVS-96, automated virus scanner operated by robotic arms
BluSense Diagnostics 12-Minute COVID-19 Test Kit Expected to receive the CE marking of the EU in May.
Academia Sinica 20 minutes rapid immune- based test kit prototype
National Health Research Institutes (NHRI) 10-15 minutes rapid diagnostic test prototype
Taiwan Advance Bio-Pharmaceutical Inc (TABP) 10-15 minutes rapid diagnostic test In-licensing from NHRI
AnTaimmu BioMed Vstrip® COVID-19 Antigen Rapid Test TW EUA submitted
iXensor two cutting-edge antigen-based testing solutions for both big-scale screening and precision diagnosing use cases in the development stage
United Biomedical COVID-19 lgG antibody test US EUA notified
TBG Diagnostics SARS-CoV-2 IgG / IgM Rapid Test Kit EU CE certification; US EUA notified
Abnova COVID-19 IgM IgG rapid test EU CE certification submitted; US EUA submitted
Excelsior Bio-System ALERT SARS-CoV-2 Antibody Rapid Test TW EUA submitted