BioPorto A/S announced an expansion of its strategic collaboration with Roche Diagnostics. As announced on December 7, 2023, BioPorto received FDA clearance in the US for its NGAL test to be marketed as ProNephro AKI (NGAL) on Roche?s cobas c 501. ProNephro AKI (NGAL) is the first Acute Kidney Injury (AKI) biomarker test cleared for pediatric use (aged 3 months through 21 years) in the US.

In continuation of the FDA approval, BioPorto and Roche Diagnostics have expanded the existing global distribution agreement for the cobas c 501 and c 502 analyzers to also include the cobas c 503 analyzer.