
Klaudia Lechowska, a business‑development specialist at Mabion Biologics, highlighted how STEM education equips women with both technical and commercial skills essential for biotech careers. She noted that women comprise about 60% of the pharma workforce but hold only a quarter of senior roles, underscoring a leadership gap. Mabion’s biosimilar MabionCD20 recently earned FDA orphan‑drug designation for membranous nephropathy and autoimmune hemolytic anemia, illustrating the company’s focus on rare‑disease therapeutics. Lechowska also emphasized emerging innovations in advanced biologics and personalized medicine as the industry pivots toward quality and safety.

Fresenius Kabi and Phlow Corp. have launched the United States’ first end‑to‑end domestic manufacturing collaboration for epinephrine injection, pairing Phlow’s new API production facility in Virginia with Fresenius Kabi’s existing formulation and fill sites. The partnership includes an FDA‑filed Drug...

The FDA granted priority review for Pfizer’s marstacimab, marketed as HYMPAVZI, to broaden its label to patients aged six and older with inhibitors and to children 6‑11 without inhibitors. Marstacimab is a weekly subcutaneous anti‑TFPI antibody, the first of its...

Integrated CDMO networks are reshaping drug development by offering end‑to‑end expertise, especially for complex modalities such as antibody‑drug conjugates (ADCs). Partnerships between specialist CDMOs allow small and mid‑size biopharma firms to access high‑potency handling, bioconjugation, and lyophilization capabilities without building...

Marcio Temtem, Hovione’s VP of Strategic Business Management, highlighted three industry shifts: growing small‑molecule complexity, faster development cycles driven by AI, and the regionalization of supply chains. Hovione counters these pressures with its amorphous solid dispersion platform, continuous flow and...

Strategic outsourcing is reshaping biopharma by linking discovery, formulation, and early‑clinical manufacturing through specialized external partners. In a Drug Digest interview, iOrganBio CEO Daniel Delubac explains how risk‑focused partner selection and integrated data flows accelerate cell, gene, and RNA therapies...

The World Economic Forum has added ACG’s Shirwal facility to its Global Lighthouse Network, making it the first pharmaceutical packaging site to receive the honor. The plant leverages AI, machine learning, IoT and digital twins to slash defects by 71%...

Elisabeth Gardiner, CSO of Tevard Biosciences, warned that women remain vastly under‑represented in pharmaceutical STEM roles, occupying only 20‑30% of such positions despite comprising half of the U.S. workforce. She highlighted a "confidence paradox" where girls' interest in STEM has...
Fujifilm Biotechnologies is hosting a free webinar titled “Shaping the Future of Microbial Development: From Gene to GMP.” The session, led by Steve Loftus, PhD, will showcase proven strategies and emerging technologies that accelerate microbial fermentation, scale‑up, and regulatory readiness....

In the latest Behind the Headlines episode, NVIDIA and Eli Lilly announced a $1 billion, five‑year AI co‑innovation lab aimed at fusing wet‑lab experiments with continuous‑learning computational models. Panelists highlighted AI’s growing role in lowering drug‑development costs and accelerating clinical‑trial timelines, moving...

IMUNON, a clinical‑stage biotech, is advancing a DNA‑mediated IL‑12 immunotherapy for advanced ovarian cancer into Phase 3 trials. The therapy uses the company’s TheraPlas nanoparticle platform to deliver an IL‑12 plasmid directly into the tumor microenvironment, converting “cold” tumors to “hot”...

Bristol Myers Squibb and Johnson & Johnson have launched the “Change the Target. Change What’s Possible” educational initiative focused on Factor XIa inhibition for thromboembolic disease. The program highlights FXIa’s potential to prevent harmful clots while preserving normal hemostasis, addressing the...

Sustainability has moved from a niche environmental concern to a core business driver for pharmaceutical manufacturers. The United States Pharmacopeia (USP), whose standards are adopted by more than 22,000 facilities in 140 countries, is leveraging its reach to embed ecological...

The European Medicines Agency has issued a recommendation for conditional marketing authorization of Sanofi Winthrop’s Rezurock (belumosudil) to treat chronic graft‑versus‑host disease in patients aged 12 and older. In an open‑label study, 73% of participants achieved a response, with 44%...

SK Capital Partners has agreed to sell the active pharmaceutical ingredient (API) assets of the Noramco Group to Swiss contract manufacturer Siegfried, as announced in a Jan 27 2026 press release. The divestiture allows Halo Pharma to become a dedicated North American...

Mirum Pharmaceuticals completed its acquisition of Bluejay Therapeutics, adding the Phase 3 antibody brelovitug for chronic hepatitis delta virus (HDV) to its pipeline. The deal integrates Bluejay’s team and assets, aiming to finish the AZURE Phase 3 program and prepare for potential...