Protein Services
GMP Manufacturing
Choose our efficient and reliable teams to complete all your cGMP batch manufacturing requirements according to applicable EMA, ICH or FDA cGMP guidelines.
Our knowledgeable technical, quality and production departments will ensure that products intended for human or veterinary use are manufactured in consistent, controlled, and reproducible processes to ensure efficacy, safety, and quality.
Drug Substance is tested by our Quality Control department using the analytical methods we have defined jointly with our customers in earlier stages and released according to the product specification by our Quality Assurance team. Each batch is accompanied by a Certificate of Analysis (CoA), a Certificate of GMP compliance and includes all relevant documentation to support clinical studies or commercial product supply.
Rely on us to ensure that your manufacturing strategy can be met with products manufactured on time and within budget.
Fill & Finish
Our solution-driven approach to supporting our customers throughout their biologics journey ensures that all Fill & Finish activities are managed in-house and according to the specifications on format, fill volume and final formulation as defined by our customer.
With you all the way…
together, making advanced biologics, and tomorrow’s life-transforming therapies.
We deliver unparalleled end-to-end development and manufacturing services for all protein expression systems and viral vectors, both for Drug Substances and Drug Products, from pre-clinical to clinical development and commercial phases.
We support our customers wherever they are on their journey, from early-stage development to commercialization. We are passionate, precise, and always close, together, making advanced biologics and tomorrow’s life-transforming therapies.
Pre-Clinical
Phase I
Phase II
Phase III
Commercial
