Pharmaceutical CDMOs in Europe are sharpening their focus on development-stage agility and sterile fill-finish capabilities while undergoing strategic reshaping to meet global demand. These Europe CDMO pharmaceutical manufacturing capsules summarize key moves from Recipharm and Lonza, including facility upgrades and divisional restructuring.
Capsule 1: Recipharm Launches Pilot-Scale Development Center in Germany
Sweden-based CDMO Recipharm announced the opening of a pilot-scale development facility in Bavaria to support oral solid dose development and scale-up. According to the company, the new site enables seamless progression from formulation to clinical supply under GMP. It includes capabilities for blending, granulation, compression, encapsulation, and coating.
Capsule 2: Recipharm Expands Blow-Fill-Seal (BFS) Sterile Platform
In a separate announcement, Recipharm said it had signed multiple new development contracts tied to its BFS platform. The company highlighted the ability to achieve over 90% API savings during formulation. The expansion is part of Recipharm’s broader strategy to support clinical-stage clients seeking cost-effective aseptic delivery systems.
Capsule 3: Lonza Reorganizes Under “One Lonza” CDMO Strategy
Lonza confirmed the restructuring of its business units under a “One Lonza” model aimed at streamlining its pharmaceutical CDMO offering. The reorg splits the company into three CDMO-focused divisions: Integrated Biologics, Advanced Synthesis (which includes small molecules), and Specialized Modalities. As part of the shift, Lonza is exiting its Capsules & Health Ingredients business. The company said this will sharpen its focus on core development and manufacturing activities.
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Sourcing Note
This article summarizes announcements and insights from publicly available press releases and corporate updates. All companies mentioned are linked to their original sources. CDMOworld.com provides editorialized coverage for informational and industry awareness purposes.
