Opera activities are ruled by internal SOPs according on SR EN ISO 9001:2015 standards. The whole personnel is trained according to ICH-GCP regulations.

The CRO developed important projects in different therapeutic areas. For the Clients that need more details, please complete the request form under confidentiality agreement.

Clinical trial related services offered by Opera include all necessary activities starting from trial sites selection, ethic-administrative submissions, monitoring and Data Management up to Statistical Analysis and Medical Writing. Opera is able to support pharmaceutical and biotech companies in the clinical development from Phase I to Phase IV and in the regulatory process for the Marketing Authorization; furthermore, Opera is involved with the development and validation of Medical Devices.

From 1995 to 2015 the company worked especially in Italy and in Western Europe. In the last years its headquarter were moved in in Romania (Timisoara), extending the clinical activities to East Europe countries.