Calao through its international network develops generics and offers APIs supporting companies in carrying out their activities on all markets through licensing, the searching for new products and partners and the preparation of registration dossiers.

Calao can coordinate non-clinical and clinical studies (BES included). Always in accordance with current GMP and GCP.

Projects are developed on tailor-made basis following customer demand, according to specific agreements.

Regulatory affairs department guarantees assistance before and during the application procedures.
Documented successful experience on MRP, DCP, centralized procedures.