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BioSynchronicity Corporation

BioSynchronicity Corporation is a USA based company founded and launched in June 2020 in the State of Washington. The global headquarters office was subsequently opened in Rochester, New York, in January, 2021.

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-administered 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 the innovative and accurate C-Sync™ COVID-19 Antigen Test, the C-SyncPlus™ COVID-19 Antigen Test, and the soon to be available C-Sync™ All-in-One COVID-19 Influenza A/B Combo Test.

The C-Sync™ family of tests look similar to a pregnancy test but are even easier to use. The science behind C-Sync™ will allow future tests for other human and pet diseases.

BioSynchronicity is a young, vigorous, and agile company leveraging experienced leadership with collectively over 400 years of expertise in global business, technology development, and healthcare delivery. Read more about our team here.

Trust & Partnership

BioSynchronicity is not a commodity company. We are a science-based solution company. We intend to earn your trust by providing rapid antigen tests that are fast, reliable, affordable, and available. Our commitment is to help people, companies, schools, event venues, hospitals, restaurants, and places that need quick health status results. This includes affluent and under-served communities alike, and both developed and developing areas around the world.

While the test can be used now for COVID-19, it may be leveraged to test for other current and future critical medical needs, such as seasonal influenza, measles, mumps, tuberculosis, pneumonia, syphilis, HIV, diabetes, and the detection of restricted drugs such as opioids.

Thus, we seek long-term relationships. We hope to build trust with the Covid C-Sync™ test to address the current pandemic. But we look forward to a long-term business relationship with new innovative products and services in the future.

Traditional Viral Diagnostic Tests vs. The BioSynchronicity Viral Diagnostic Tests

There are two types of diagnostic tests for viral pathogens:

  • Those that target host antibodies produced in response to viral infection
  • Those that target the virus’s genome.

Antibody-based tests (also known as serological tests) require blood to be drawn from infected individuals several days after viral transmission to give their immune system enough time to produce IgA, IgM, and IgG antibodies. Antibody tests are essential for identifying individuals who have already been infected during a pandemic and have since recovered, especially those who never developed symptoms.

Nucleic acid-based tests only require the presence of the virus itself. Since these tests can detect viruses in patient samples even before symptom onset, nucleic acid-based tests are used instead of antibody-based tests to combat viral spread. The most common nucleic acid-based tests rely on real-time polymerase chain reaction (RT-PCR) to amplify reverse-transcribed viral RNA. These tests are not without their shortcomings. Subpar sample handling can lead to false negatives, and amplification proceeds slower than isothermal amplification technologies such as loop-mediated amplification (LAMP). Because samples are usually shipped to a centralized laboratory for testing, RT-PCR tests can take over a day to as many as two weeks in pandemic times from collection to result. Laboratory RT-PCR tests also require trained technicians to carry out the protocol and interpret the results.

BioSynchronicity is focused on point-of-care (POC) testing (i.e., testing in the field rather than a laboratory) and home self-testing where authorized by local regulatory bodies. Scientists generally agree that a frequent and consistent regimen of POC testing is essential to fight the spread of highly contagious viruses, as it allows rapid identification of infected patients to enable isolation and efficient contact tracing. Although point-of-care RT-PCR diagnostics exist, they have been superseded by tests that use more rapid amplification technologies (e.g., LAMP) and smaller instruments. New high sensitivity Lateral Flow Assays from BioSynchronicity using a simple nasal sample. In development are systems which will use a saliva sample as a biological specimen, offer significant advantages over traditional diagnostic testing for viruses, pathogens, and bacteria. They are affordable, accurate, do not require trained technicians, do not require additional laboratory equipment, and are easy to use with easily interpreted rapid results in minutes.

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