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Sandoz Raises 2026 Core-EBITDA Margin Outlook to 23.0–23.5%

By Drooid · · How we work

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  • After the EMA created a dedicated biosimilar pathway in 2003, Europe authorized its first follow-on biologics and, since 2006, has granted marketing authorisations for over 50 biosimilars, including the EU’s first monoclonal-antibody copy in 2013. Building on that framework, Sandoz opened a high-volume biosimilar drug-substance centre in Slovenia in 2026, expanding its pipeline under the same regulatory regime.
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