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Podcast: Keeping IT Brief
Episode: An FDA Look at Challenges in Health Laboratory Data Interoperability
Description: In early June of last year, HHS announced new laboratory data reporting guidance for COVID-19, citing LOINC In Vitro Diagnostic (LIVD) as the authoritative source of coding for COVID-19 testing. With the number of daily COVID-19 tests continuing to go up in the United States, Dr. Greg Pappas, Associate Director for National Device Surveillance, Center for Devices and Radiological Health, Food & Drug Administration discusses how the LIVD catalog improved public health reporting for COVID-19 test results.About Greg PappasAs the Associate Director for National Device Surveillance at FDA, Dr. Pappas has played...