Trinity Biotech launches FDA-cleared preeclampsia test service

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Go back to Trinity Biotech launches FDA-cleared preeclampsia test service

Trinity Biotech Announces Launch of FDA-cleared Preeclampsia Testing Service

August 7, 2025 8:01 AM EDT

FDA-cleared PreClara Ratio (sFlt-1/PlGF) biomarker test offers clinicians a crucial tool for managing hypertensive disorders of pregnancy, with potential significant cost savings and improved patient outcomes

DUBLIN, Aug. 07, 2025 (GLOBE NEWSWIRE) -- Trinity Biotech plc (Nasdaq: TRIB), a commercial-stage biotechnology company focused on human diagnostics and diabetes management solutions, including wearable biosensors, today announced the launch of a new testing service for preeclampsia, a significant advancement in maternal health diagnostics. The service is planned to be rolled out in Q3 2025 through Trinity Biotechs New York-based reference laboratory.

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