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Biose Industrie does not develop its own therapeutics but serves as a world-leading CDMO specializing in the process development, scale-up, and GMP manufacture of live biotherapeutic products and next-generation probiotics for clients globally. The company supports projects from preclinical through commercial launch stages. It has demonstrated expertise in regulatory compliance with ANSM, EMA, FDA standards. Clinical results pertain to client programs manufactured by Biose.
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