Tag Archives: FDA

San Clemente, CA – March 18, 2021 — The IVD Industry Connectivity Consortium today announced the release of LOINC® to Vendor IVD (LIVD) Specification V2.0. LIVD outlines an industry-defined format to facilitate the publication and exchange of LOINC codes for vendor IVD test results, based on either vendor IVD test transmission codes or manual test…

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FDA encourages the adoption of the IVD Industry Connectivity Consortium’s LIVD format for distribution of LOINC codes for IVD tests

The US Food and Drug Administration published a Guidance for Industry and Food and Drug Administration Staff, titled ”Logical Observation Identifiers Names and Codes for In Vitro Diagnostic Tests” in which it encourages the adoption of the IVD Industry Connectivity Consortium’s LIVD format for distribution of LOINC codes for IVD tests. The FDA recognizes LIVD…

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IVD Industry Connectivity Consortium announces LIVD specification for digital publication of LOINC to vendor IVD test results in clinical laboratories

By: IVD Industry Connectivity Consortium Chicago, IL – June 1, 2017 –  The IVD Industry Connectivity Consortium (IICC) today announced the LIVD specification for digital publication of LOINC to vendor IVD test results in clinical laboratories. Along with the IICC/IHE LAW Profile -soon to be recast as CLSI AUTO16- LIVD allows IVD instruments and IVD…

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