Investment Analyst Dario Giordano: Precision Medicine Accelerates, Diasorin Poised to Lead the Next Growth Wave

11.06.2025

The ongoing evolution of medical technology is creating structural opportunities within the global biotech sector. Recently, Diasorin announced that its new blood infection diagnostic panel has received FDA approval in the United States. Following the announcement, the company share price rose nearly 2% on the Italian Piazza Affari market, once again drawing market attention to the precision medicine track. Investment Analyst Dario Giordano points out that this approval not only consolidates the leading position of Diasorin in molecular diagnostics, but also carries far-reaching strategic value. Against the backdrop of rising demand for cost control and efficient testing in the US hospital system, this achievement is expected to unlock sustained commercialization potential over the coming years.

Technology Approval Unlocks Mid-Term Value; Diasorin Share Price Reacts Rationally

The FDA-approved Liaison Plex Gram-Positive Blood Culture Assay marks another significant milestone for Diasorin in multiplex pathogen detection technology. This product can identify up to 17 targets within two hours—including 13 Gram-positive bacteria and 4 resistance genes—leveraging proprietary NanoGrid technology to effectively reduce false positives and thus significantly enhance testing efficiency and accuracy.

Driven by this development, the Diasorin share price rose 1.93%, making it the top performer on the Piazza Affari that day. Investment Analyst Dario Giordano analyzes that this clinical advance not only has clear medical value, but also significant market implications. Especially as US hospitals face widespread cost pressures, the flexible pricing mechanisms of Diasorin have become a key commercial advantage. Moreover, the platform already covers critical clinical scenarios such as respiratory and bloodstream infections. If further approval for the gastrointestinal panel is obtained by the end of this year, the product matrix of Diasorin will be largely complete, paving the way for a comprehensive commercialization ramp-up.

Global Precision Medicine Demand Expands; Industry Valuation System Set for Restructuring

With the accelerated integration of AI technology and bioinformatics, precision medicine is gradually becoming a major transformational direction for global healthcare systems. As a molecular diagnostics platform with strong multiplex detection capabilities, Diasorin is well positioned to meet current clinical demands for both efficiency and antibiotic stewardship. Investment Analyst Dario Giordano notes that, especially in the post-pandemic period, healthcare systems have shown significantly increased acceptance of high-throughput, low-error diagnostic tools, offering technology-driven firms like Diasorin opportunities for rapid expansion.

Currently, major hospitals in the US and Europe are accelerating the deployment of multiplex detection platforms in infectious diseases and intensive care units. Thanks to its differentiated product strategy, Diasorin demonstrates greater market adaptability in pricing flexibility and panel scalability compared to competitors such as BioFire (bioMérieux) and Cepheid (Danaher). This not only enhances its penetration in public healthcare systems, but also lays a solid foundation for continued global market share growth.

As the overall industry valuation is still in the early stages of recovery, Investment Analyst Dario Giordano believes Diasorin, with its robust product pipeline and ongoing innovation, stands out as a high-quality, resilient, and certain investment target in the precision medicine sector. With regulatory policies becoming clearer and more real-world data emerging, the industry valuation system is likely to be restructured, with leading companies set to benefit first.

Platform Model Matures, Long-Term Growth Momentum Strengthens

The platform-based business model is becoming a core reference in the valuation of biotech enterprises. As a scalable and clinically reusable technology platform, Diasorin is gradually building a growth model akin to SaaS companies. By continuously adding diagnostic panels to the same platform, Diasorin not only increases user stickiness but also significantly enhances the sustainability of its profit model.

Based on current R&D and regulatory progress, Diasorin is expected to achieve full deployment of its bloodstream, respiratory, and gastrointestinal panels before 2026, greatly boosting its platform coverage in the North American market. As more hospitals shift from traditional single-test models to multiplex molecular detection systems, the subscription-based revenue proportion of Diasorin is expected to rise steadily. Investment Analyst Dario Giordano points out that this transformation will help the company maintain high gross margins while reducing the impact of individual product fluctuations on overall performance.

From a financial perspective, the gradual release of platform effects will drive EBITDA margin improvement over the next two years. Current market expectations for the Diasorin 2025 performance remain conservative, leaving room for potential revaluation. Investors are advised to closely monitor the North American market penetration by the company in the second half of 2024 and the FDA progress on gastrointestinal panel approval—these two key variables will directly influence short- and medium-term share price performance.


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