Medace is committed to bring the (bio)medical innovations (ATMPs, biopharmaceuticals & medical devices) of start-ups and academics to the market and patients faster. By sharing our expertise, infrastructure, Quality Management System (QMS), and equipment we improve product quality, increase efficiency, and reduce costs. We offer start-ups and researchers flexible access to our 2,000 m2 R&D and Cleanroom facilities to enable them to perform development and clinical-grade production of their product when needed. Clients are also guided in how to set-up their technical dossier and QMS required for clinical validation by our regulatory and quality experts. We have an overarching QMS in place, offer specialized infrastructure (incl. 12 Cleanrooms, GMP grade D to B), validated equipment, dedicated training programs and trained professionals for hands-on guidance and support. The Medace approach, infrastructure and QMS are certified according to the latest standards and compliant to the pharmaceutical guidelines.