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Mar 30, 2020PRESS STATEMENT 30 March 2020 The Food and Drug Administration (FDA) approves the use of five (5) Rapid Test Kits for COVID-19 today, March 30, 2020. The FDA supports all efforts to address this pandemic. These point-of-care test kits are registered for use in countries with reliable regulatory agencies such as China and Singapore. We fast delivery igm rapid test kit certified output manilaRead more »FDA Advisory No. 2020-483 |FDA APPROVES RAPID Mar 30, 2020In line with the ongoing response to the increasing number of COVID-19 cases in the Philippines, the Food and Drug Administration (FDA)- Philippines hereby provides an initial list of approved Rapid Antibody Test Kits. PRODUCT NAME MANUFACTURER 1. NANJING VAZYME 2019-nCoV IgG/IgM DETECTION KIT Biolidics Limited. 37 Jalan Pemimpin, #02-07, Mapex, Singapore 2.FDA Advisory No. 2020-483 |FDA APPROVES RAPID Mar 30, 2020In line with the ongoing response to the increasing number of COVID-19 cases in the Philippines, the Food and Drug Administration (FDA)- Philippines hereby provides an initial list of approved Rapid Antibody Test Kits. PRODUCT NAME MANUFACTURER 1. NANJING VAZYME 2019-nCoV IgG/IgM DETECTION KIT Biolidics Limited. 37 Jalan Pemimpin, #02-07, Mapex, Singapore 2.

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Mar 31, 2020MANILA, Philippines The Food and Drug Administration (FDA) announced yesterday the approval of the use of five rapid antibody test kits for coronavirus disease 2019 (COVID-19).FDA approves 5 rapid test kits for virusMANILA, Philippines The Food and Drug Administration (FDA) announced yesterday the approval of the use of five rapid antibody test kits for coronavirus disease 2019 (COVID-19). At a press fast delivery igm rapid test kit certified output manilaFDA approves 5 rapid test kits for virusMANILA, Philippines The Food and Drug Administration (FDA) announced yesterday the approval of the use of five rapid antibody test kits for coronavirus disease 2019 (COVID-19). At a press fast delivery igm rapid test kit certified output manila

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Some results are removed in response to a notice of local law requirement. For more information, please see here.Some results are removed in response to a notice of local law requirement. For more information, please see here.FDA Advisory No. 2020-483 |FDA APPROVES RAPID

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