BioSynchronicity Corporation is an SBA certified Woman Owned Small Business (WOSB) launched in June 2020 in the State of Washington. The focus of the BioSynchronicity team is the design, development, research, validation, manufacturing, and commercialization of in vitro, clinical diagnostic, and forensic tests and devices for the health of humans, animals, and the ecosystem.
At the time of its launch, BioSynchronicity was tasked with designing and developing a reliable, simple, affordable, widely-available, and ultra-rapid SARS-CoV-2 antigen diagnostic test for hospital and point of care (POC) use, school and business screening programs, as well as self-administed testing at home through over-the-counter (OTC) sales where authorized by regulatory bodies.
To meet this challenge, a global team of like-minded scientists, doctors, engineers, and other seasoned international business professionals was assembled, resulting in the creation of our first test: the C-Sync® COVID-19 Antigen Test, a multi-target test to detect SARS-CoV-2. The C-Sync® COVID-19 Antigen Test received an EUA in March 2023. Our team has leveraged our innovative C-Sync® platform to develop new diagnostic tests.
BioSynchronicity has received an Emergency Use Authorization from the FDA (EUA220346) for its flagship lateral flow assay (LFA), the C-Sync® COVID-19 Antigen Test. The C-Sync® assay platform is readily adaptable to the detection of a broad spectrum of viral and bacterial infections. Highly accurate and sensitive rapid forensic singleplex and multiplex tests for the detection of Fentanyl, Xylazine, and other opioids and illicit drugs are available for Harm Reduction programs, as well as for employee drug screening and insurance testing. Test device customization, private label, and OEM options are available.
A new series of innovative diagnostic tests dedicated to improve women’s and neonatal health are also in development.