FDA Issues Letter to Healthcare Providers as Patient COVID-19 Self-Collection Affects Specimen Quality
Three teaching points for self-collecting SARS-CoV-2, COVID-19 specimens; FDA cautions healthcare providers about poor specimen quality.
COVID-19 Business Intelligence and Analysis for Clinical Laboratories, Pathology Groups and Hospital Administration
Reliable COVID-19 Business Intelligence and analysis for clinical laboratories, pathology groups and Laboratory Diagnostics.
Three teaching points for self-collecting SARS-CoV-2, COVID-19 specimens; FDA cautions healthcare providers about poor specimen quality.
Quick links to clarification of CMS policy for clinical laboratories and updated FDA recommendations to healthcare providers about antigen testing of certain asymptomatic individuals.
A six-point primer to the new CMS clinical laboratory CLIA quick start guide released in September 2020.
With 47 COVID-19 antibody tests authorized for use under FDA EUA as of Sept. 24, 2020, only one is authorized as POC for fingerstick blood samples collected in patient care settings.
Lowest limit of detection noted.
Three essential points pertaining to university laboratories planning for SARS-CoV-2 surveillance testing.
Three teaching points for self-collecting SARS-CoV-2, COVID-19 specimens; FDA cautions healthcare providers about poor specimen quality.
Quick links to clarification of CMS policy for clinical laboratories and updated FDA recommendations to healthcare providers about antigen testing of certain asymptomatic individuals.
A six-point primer to the new CMS clinical laboratory CLIA quick start guide released in September 2020.
With 47 COVID-19 antibody tests authorized for use under FDA EUA as of Sept. 24, 2020, only one is authorized as POC for fingerstick blood samples collected in patient care settings.
Lowest limit of detection noted.
Three essential points pertaining to university laboratories planning for SARS-CoV-2 surveillance testing.