CMS Releases New COVID-19 Testing and Reporting Requirements
Guidance released Sept. 8 provides simplified details on nursing home testing that should be performed, also identifies three circumstances related to COVID-19 testing triggers.
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.
Guidance released Sept. 8 provides simplified details on nursing home testing that should be performed, also identifies three circumstances related to COVID-19 testing triggers.
Four key points from the FDA’s September 2020 update to initial COVID-19 convalescent plasma guidelines.
Combination coronavirus flu tests readying for flu season.
Details fall into place for invoking the Defense Production Act for SARS-CoV-2 antigen test production.
Points of interest from CMS-3401-IFC and CLIA requirements modified in August 2020.
New guidance for those seeking approval or clearance of, or an EUA for, an LDT, and for those opting to use LDTs in their laboratories without FDA premarket review or authorization.
Guidance released Sept. 8 provides simplified details on nursing home testing that should be performed, also identifies three circumstances related to COVID-19 testing triggers.
Four key points from the FDA’s September 2020 update to initial COVID-19 convalescent plasma guidelines.
Combination coronavirus flu tests readying for flu season.
Details fall into place for invoking the Defense Production Act for SARS-CoV-2 antigen test production.
Points of interest from CMS-3401-IFC and CLIA requirements modified in August 2020.
New guidance for those seeking approval or clearance of, or an EUA for, an LDT, and for those opting to use LDTs in their laboratories without FDA premarket review or authorization.