The complexity of compounding the patient-specific therapies requires high-level expertise and outstanding technological equipment. Our trained staff works in state-of-the-art cleanroom labs where they follow the highest quality and safety standards of Good Manufacturing Practice (GMP) and use only pharmaceutical products approved in Germany. The portfolio currently includes ready-to-use infusions for cytostatic therapy, antibody solutions, and clinical investigational medicinal products.

Medios Solutions Berlin holds the manufacturing license under §13 of the German Medicines Act (AMG), as well as the wholesale license under §52a AMG. The versatile technological equipment in our state-of-the-art cleanrooms includes, among other things, an H₂O₂ airlock. We also have well-established paperless processes and an electronic quality management system (eQMS). This allows our customers to benefit from the highest safety and reliability throughout the entire process, from order placement to delivery. 

Thanks to our strategically planned storage and logistics system, as well as our network within the Medios Group across Germany, we respond extremely quickly and adapt seamlessly to customers' needs.