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Pharmaceuticals & Biotech

Danaher’s Beacon Program Accelerates Academic Innovation into Scalable Real-World Impact

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SHERIDAN, WYOMING – May 17, 2025 – Danaher Corporation is reinforcing its position at the forefront of life sciences and diagnostics innovation through its Beacon program—an initiative designed to transform cutting-edge academic research into scalable, market-ready solutions. Spearheaded by Vanessa Almendro, PhD, MBA, Vice President, Head of Science and Technology Innovation at Danaher, the Beacon model exemplifies how strategic academic-industry collaboration can generate high-impact innovations aligned with real-world healthcare and biotechnology challenges.

Danaher’s Science Chief Reaffirms Confidence in Healthcare Innovation Amid Industry Headwinds

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SHERIDAN, WYOMING – May 17, 2025 – Despite facing one of the most turbulent periods since the biotech industry’s inception in the 1970s, Danaher’s Chief Science Officer, Jose-Carlos Gutierrez-Ramos, believes the sector stands on the cusp of unprecedented progress. In a new commentary, Gutierrez-Ramos outlines why the healthcare and life sciences industries should remain optimistic, citing the explosive growth of GLP-1 receptor agonists, a rapidly evolving pipeline in Alzheimer’s research, and the transformative power of artificial intelligence.

Danaher Underscores RNA Medicine Advancements, Urges Continued Industry-Wide Investment

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SHERIDAN, WYOMING – May 17, 2025 – Danaher Corporation is spotlighting the rapid progress and growing potential of RNA medicines, reaffirming its strategic commitment to genomic innovation while calling on industry stakeholders to sustain investment in the field. As RNA therapeutics expand across disease areas and delivery methods, Danaher’s leadership is urging the life sciences ecosystem to double down on momentum at what it describes as a defining moment for RNA-based medicine.

Breakthroughs in RNA Delivery and Safety Optimization

CHMP Recommends EU Label Update for Roche’s Phesgo to Allow Administration Outside of Clinical Settings

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SHERIDAN, WYOMING – May 8, 2025 – Roche has announced that the European Medicines Agency’s Committee for Medicinal Products for Human Use (CHMP) has issued a positive opinion recommending an update to the European Union (EU) label for Phesgo®, a subcutaneous (SC) fixed-dose combination of Perjeta® (pertuzumab) and Herceptin® (trastuzumab), used for treating HER2-positive breast cancer. The label update will allow for Phesgo to be administered outside of clinical settings, such as at patients’ homes, under the supervision of a healthcare professional.