We are a high profile CRO established for the management and conduction of excellence of clinical studies of high technical and scientific content, requiring special regulatory and clinical care.
We are a well established and dynamic group, in continuous education and training, and in continuous search for innovative solutions, stimulated by problems that challenge problem solving abilities.
Our characteristics are team working, dynamic flow of information and true attention to training and updating.
We operate with rigour and flexibility at the same time, in continuous contact and co-operation with sites and sponsor, achieving sound results in full compliance with ICH-GCP and all international and local rules and regulations.
Our services are addressed to sponsors who believe that outsourced clinical studies must be managed with the same care and personalisation which would have been dedicated by the sponsor, with effective and continuous reciprocal contributions. We offer tailored services of excellence, as different clinical trials and different sponsor needs require equal care but personalised solutions.
- start up, Ethic Committee regulatory submissions
- clinical trial management
- medical management
- data management
- writing scientific paper and bibliographic searches
- financial and legal aspects of clinical trials
- clinical trial monitoring (remote and onsite)
- training
- statistics
- meetings
- medical scientific translations
- medical writing