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European Pharmaceutical Contract Manufacturing Market to Reach $108.1 Billion by 2035

Published: May 2026

European pharmaceutical contract manufacturing market is driven by the increasing outsourcing of drug development and manufacturing activities by pharmaceutical and biotechnology companies, aiming to reduce operational costs and improve production efficiency. The growing demand for complex biologics, personalized medicine, and advanced drug formulations is further accelerating the adoption of contract manufacturing services across Europe. Additionally, stringent regulatory compliance requirements and the need for high-quality manufacturing standards are encouraging companies to partner with specialized contract development and manufacturing organizations (CDMOs) to ensure scalability, reliability, and faster time-to-market.

Browse the full report description of “European Pharmaceutical Contract Manufacturing Market Size, Share & Trends Analysis Report, By Manufacturing Process Type (Sterile Manufacturing, and Non-Sterile Manufacturing), By Product Type (OTC, API, Finished Dosage Formulation, and Others), By Route of Administration (Oral, Inhaled, Parenteral, and Others), By Service (R&D, Manufacturing, and Non-Clinical), Forecast Period (2026-2035)” at https://www.omrglobal.com/industry-reports/european-pharmaceutical-contract-manufacturing-market

Sandoz expands European biosimilar manufacturing (2025)


Sandoz Group AG completed the acquisition of Just-Evotec Biologics EU SAS (Toulouse site) in 2025, significantly strengthening its biosimilars manufacturing and development capabilities in Europe. The acquisition enhances Sandoz’s internal biologics production capacity and integrates advanced continuous manufacturing technologies, improving efficiency and scalability in biologics production. This move also expands the company’s European manufacturing footprint, particularly by reinforcing operations across Slovenia and France, thereby supporting a more integrated and resilient biosimilars supply network in the region.

NextPharma divests logistics to focus pure CDMO model (2025)


In 2025, NextPharma divested its logistics business as part of a strategic shift toward becoming a pure-play Contract Development and Manufacturing Organization (CDMO). This restructuring allows the company to concentrate entirely on pharmaceutical manufacturing services across key dosage forms, including solid, semi-solid, sterile, and non-sterile products. The decision strengthens NextPharma’s specialization within Europe’s CDMO landscape by streamlining operations and focusing on core manufacturing capabilities, aligning with growing demand for outsourced pharmaceutical production.

Siegfried expands Swiss CDMO operations (2025)


Siegfried, a Switzerland-based CDMO, expanded its European manufacturing operations in 2025 through increased investments in both active pharmaceutical ingredient (API) and finished drug product manufacturing sites. The expansion particularly strengthens its high-potency API production capabilities, driven by rising demand from European pharmaceutical clients. This capacity enhancement supports more robust and compliant supply chains across regulated European markets, reinforcing Siegfried’s position in high-value, specialized pharmaceutical manufacturing services.

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