CDMO

Experienced partner in the aseptic processing of injectables

Since our founding in 1970, we have believed in local and European production and have never considered relocating our manufacturing facilities to non-European countries. This dedicated geographical focus enables us to offer our reliable and highest-quality production assets to partners.

The expansion of our contract development and manufacturing organisation (CDMO) is another important business area at medac. Our company is an experienced partner in the aseptic processing of injectables. Specialised in the sterile manufacture of medicinal products in the clinical and commercial sectors for global markets, we offer customised solutions and comprehensive services. Our expertise includes the formulation and filling of sterile injectables, the manufacture of high and low potency molecules as well as conventional and complex sterile manufacturing services.

With over 20 years of experience in complying with global standards such as FDA, ANVISA and PMDA, we guarantee the highest quality and reliability. Our flexible high-speed filling lines enable the production of a wide range of pre-filled syringes and injection vials. Our customers benefit from short lead times and our technological expertise in the field of technology transfer. We support them with our expertise throughout the entire product life cycle.