With R&D, production and regulatory affairs all integrated on a single site we offer a complete range of CDMO services from early-stage development to scale-up & commercial manufacture of high potent APIs with occupational exposure limits (OEL) down to 0.1g/m³/shift (OEB class 5). In trusted long-term partnerships, we enable pharmaceutical and biotechnological companies to develop and provide innovative treatments of the highest quality to their patients globally. We have a proven track record in our capability to take projects from early stage through to commercial production. We operate three FDA inspected sites in France and Belgium.
Drugs in Development
KEY PRODUCTS
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Active Pharmaceutical Ingredients
Finished Drug Formulations
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CDMO (API & HPAPI)/ Generics/ Security of supply/ Regulatory submission expertise/ Track record performance/ FDA & GMP
