Feb 7, 2023
FDA
The new article covers the matters related to antigen diagnostic tests and explains the approach to be applied by the test developers in order to ensure the continued effectiveness of their devices. Table Of Contents: The Food and Drug Administration (FDA or the...
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Feb 7, 2023
FDA
The new article highlights the key points related to molecular diagnostic tests and describes the recommendations provided by the authority in this respect. Table Of Contents The Food and Drug Administration (FDA or the Agency), the UA regulating authority in the...
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Feb 7, 2023
FDA
The new article highlights the aspects related to the way the impact of viral mutations can be addressed when developing tests. Table Of Contents: The Food and Drug Administration (FDA or the Agency), the US regulating authority in the sphere of healthcare products,...
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Feb 2, 2023
FDA
The article describes the approach to be applied with respect to viral mutations and their potential impact on the performance of tests intended to identify the virus. Table Of Contents: The Food and Drug Administration (FDA or the Agency), the US regulating authority...
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Oct 22, 2020
MHRA
The Medicines & Healthcare products Regulatory Agency (MHRA), the UK regulating authority in the sphere of medical devices, has published the Target product profile (TPP) for the tests intended for the point of care use to detect the virus SARS-CoV-2 (the “novel...
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