Trinity Biotech Secures Key Regulatory Approval for Offshored and Outsourced Manufacturing of Its Flagship Rapid HIV Test, Accelerating Strategic & Financial Performance Transformation

Core Insights - Trinity Biotech has received WHO approval for offshored and outsourced upstream manufacturing of its TrinScreen™ HIV rapid test, a significant step in its transformation plan aimed at improving financial performance and achieving sustainable profitability [1][6]. Group 1: Manufacturing Transition - The approval allows Trinity Biotech to shift production from in-house operations to a more cost-effective and scalable outsourced model, ensuring product integrity and regulatory compliance [2]. - The transition is expected to unlock significant cost efficiencies, enhance operational agility and scalability, and improve gross margins and working capital [3][6]. Group 2: Strategic Objectives - This move is part of a broader strategic initiative to streamline operations, reduce fixed costs, and focus on innovation and market expansion [3]. - The new manufacturing model for TrinScreen™ HIV is set to be implemented in Q3 2025, marking a critical phase in the company's transformation journey [4]. Group 3: Company Overview - Trinity Biotech is a commercial-stage biotechnology company focused on human diagnostics and diabetes management solutions, including wearable biosensors [8]. - The company develops and markets diagnostic systems for point-of-care and clinical laboratory segments, with a presence in over 75 countries worldwide [8].