OPIS offers a full range of integrated clinical research services to pharmaceutical, biotechnological and medical device industries. With 10 locations in Europe and a huge network of monitors, OPIS offers scientific advice, trial start-up, monitoring, study management, data management, statistics, pharmacovigilance as well as quality assurance and training.
The company specializes in e-Clinical services and its in-house developed and web-based CLINICAL.NET is fully validated and FDA 21 CRF Part 11 compliant. A highly customizable, modular platform allows for user-friendly interface with validated systems of Sponsors, central laboratories, imaging providers and even mobile and wearable devices to integrate and facilitate e-Data Capture.
With significant experience in the major therapeutic areas and more than 1100 trials completed, OPIS guarantees quality, ISO 9001 and ISO 27001 compliant services in line with Good Clinical Practice (ICH-GCP) guidelines and standard operating procedures (SOP).
Our priority is to protect the rights, the safety and the welfare of the patients as well as ensuring the integrity, transparency and reliability of data collected.
We are passionate about what we do and we want our name to stand for Excellence.
Clinical Solutions Director
Phone: +39 0362 633 381