ESTEVE CDMO is a global pure-play development and manufacturing partner, specialized in high-quality small-molecule APIs, high-potent APIs (HPAPIs), and advanced pharmaceutical intermediates for innovative pharma and biotech companies.

With 55+ years of experience and 6 cGMP-certified sites across the USA, Spain, Mexico, and China, we deliver end-to-end solutions from pre-clinical development to commercial manufacturing. Our expert team, combined with cutting-edge technologies and state-of-the-art facilities, ensures flexibility, reliability, and full compliance with complex regulatory requirements.

Our customer-centric approach, led by a dedicated Project Manager and cross-functional team of experts, guarantees seamless communication, proactive problem-solving, and on-time delivery. By combining our collaborative approach with proven expertise in advanced technologies, we successfully navigate complex
projects and consistently deliver high-quality results.

At ESTEVE CDMO, our commitment is clear: to help our partners bring life-changing therapies to patients worldwide by solving their most complex challenges with precision and care.

Services

• Custom API Development and Manufacturing
• Spray Drying End-to-End Services
• CMC Supporting

Solutions

• From Preclinical to Commercial Manufacturing
• Process and Analytical Development
• Solid Form and Particle Design
• Process Engineering