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The Potential Role of Rapid Antibody Assays in the Assessment of SARS-CoV-2 Vaccine Efficacy

The Potential Role of Rapid Antibody Assays in the Assessment of SARS-CoV-2 Vaccine Efficacy

by Frederick Schaffer, MD | Sep 25, 2020 | Research

Evaluating SARS-CoV-2 Vaccine Efficacy With Rapid Antibody Assays More than 180,000 deaths have occurred in the U.S.A. due directly to COVID-19 and/or associated complications. Remarkable advancement in diagnostics and treatment have been achieved to date, but further...
Corroboration of the Accuracy of the Biohit SARS-CoV-2 IgM/IgG LFA Test Kit

Corroboration of the Accuracy of the Biohit SARS-CoV-2 IgM/IgG LFA Test Kit

by Frederick Schaffer, MD | Jun 8, 2020 | Research

Corroboration of the Accuracy of the Biohit SARS-CoV-2 IgM/IgG LFA test kit The human immune response to a COV/0-19 infection encompasses the host synthesis of anti-SARS-CoV-2 lgM antibodies that are detectable after about 5 to 7 days of infection which, in turn, is...
Dr. Schaffer Discusses the Different Types of Covid-19 Tests and How the Detection Process Works.

Dr. Schaffer Discusses the Different Types of Covid-19 Tests and How the Detection Process Works.

by Frederick Schaffer, MD | Jun 6, 2020 | Research

COVID-19 Testing and Detection: How It Works [Transcript of Video] Dr. Frederick Schaffer Explains COVID-19 Testing and Detection Hello, I’m Dr. Fred Schaffer, and I’m a board-certified allergist immunologist and a former university associate professor....
Corroboration of the Accuracy of the Biohit SARS-CoV-2 IgM/IgG LFA Test Kit

The Administration of Convalescent Plasma to Patients with COVID-19 Infections

by Frederick Schaffer, MD | Jun 3, 2020 | Research

by Frederick M. Schaffer, M.D., Paul V. Holland, M.D. and James D. Strader, D.C. Introduction: COVID-19 cases have been documented in over 188 countries.  Unfortunately, many high risk patients develop significant morbidity which in turn may result in death. Both...

Our organization striclty adheres to FDA policies and regulations covering the sale of diagnostic testing supplies for COVID-19. While personal protective equipment (PPE) may be purchased without restriction, consistent with current FDA CLIA guidance, we restrict sales of diagnostic tests to medical professionals qualified to use these kits on site.

FDA Policy for Diagnostic Tests for Coronavirus Disease-2019

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