Class I, IIa, IIb and III medical devices, provided with the CE mark, are designed and manufactured by the Medical Device Division.

The manufacturing environments have 300kg – 1000kg – 1500kg – 2500kg reactors, designed thanks to the latest technology to satisfy and guarantee the manufacturing needs of the most structured clients while remaining flexible for the manufacturing of small and pilot lots.

The service can also cover the compilation of the Technical Dossier, supporting scientific rationale, research of supporting scientific studies, notification of the Medical Device and support for the authorization of the Ministry of Health to the health advertising.

The available pharmaceutical forms are: tablets, capsules, SDC cap, liquids, spray, creams and gel.