We can take your pharmaceuticals from lab scale to the early clinical phase and beyond. Our state-of-the-art facility, with GMP-compliant clean rooms, is well equipped to offer a wide range of analytical testing and regulatory support. These services are tailored to your specific needs, implementing the relevant quality guidelines at every step along the way.

Manufacturing, testing and distribution of investigational medicinal products (IMPs) is strongly regulated by the relevant authorities to assure high quality when administered to patients in clinical trials. Full transparency and traceability, from the origin of the starting materials to dosing and the ultimate destruction of the study medication, all in compliance with Good Manufacturing practices (GMP), is mandatory. Maintaining a GMP-certified status for clean rooms requires continuous investment in equipment, facilities and well-trained people.