Detailed guide: Lateral flow validation prioritisation criteria for rapid diagnostic assays for specific SARS-CoV-2 antigens

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Published 8 February 2021
Last updated 6 April 2021 +show all updates

  1. Updates to the self-testing section with links to more detail on the CE mark, UKCA mark and MHRA exemptions from medical devices regulations.

  2. Update on sample types required for validation of lateral flow devices.


  3. First published.


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