We can arrange the contract manufacturing of small batches of investigational materials for phase I and II clinical trials
Coordinated clinical management
We can supervise the formulation, manufacturing and release of these products to multiple locations across Europe, according to your needs.
When required, our skilled teams can also provide you with advice and assistance in completing relevant parts of the regulatory dossier submission.
We can also develop intermediate suspension products, creams and liquid ointments, suspensions and powder-capsule products.
All the contract manufacturing sites we use adhere to Good Manufacturing Practice (GMP) for assurance of quality control and high standards.