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BioPorto Receives FDA 510(k) Clearance for NGAL Test in the

BioPorto Receives FDA 510(k) Clearance for NGAL Test in the
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United statesAshleyr robinsonPrasad devarajanDrug administrationBioporto company announcementsGlobal press relationsPatients agedAcute kidney injuryTony pareChief executiveSenior medical directorDevelopmental biologyDialysis unitCincinnati childrenHospital medicalRoche diagnostics gmbh

BioPorto Receives FDA 510(k) Clearance for NGAL Test in the United States First Test to Aid in Assessing AKI Risk for Patients Aged 3 Months Through 21 Years -December 07, 2023 at 04:23 pm EST

December 7, 2023 Announcement no. 20 BioPorto Receives FDA 510 Clearance for NGAL Test in the United StatesFirst Test to Aid in Assessing AKI Risk for Patients Aged 3 Months Through 21 Years .

United statesAshleyr robinsonPrasad devarajanGlobal press relationsDrug administrationBioporto company announcementsPatients agedAcute kidney injuryTony pareChief executiveSenior medical directorDevelopmental biologyDialysis unitCincinnati childrenHospital medicalRoche diagnostics gmbh

BioPorto Initiates Search for new CFO as Neil Goldman Resigns -September 19, 2023 at 09:17 am EDT

September 19, 2023Announcement no. 15 BioPorto Initiates Search for new CFO as Neil Goldman Resigns COPENHAGEN, DENMARK and BOSTON, MA, USA, September 19, 2023, – BioPorto A/S announced.

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Bioporto Provides Update On Ngal Test Regulatory Pathway

Bioporto Provides Update On Ngal Test Regulatory Pathway
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United statesBioportoas bioportoAshleyr robinsonTim eriksenDrug administrationProvides updateBurdensome provisionsTony pareChief executive officerAcute kidney injuryNasdaq copenhagenInterim reports

BioPorto A/S announces results of rights issue

BioPorto A/S announces results of rights issue
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United statesBioportoas bioportoTim eriksenDanish business authorityDrug administrationTony pareChief executiveNew sharesNasdaq copenhagenDanish businessZenith advisoryAcute kidney injuryInterim reports