and give the best value to your clinical trials
The group pursues a clear and definite aim: to support sponsors and investigators in contributing to the scientific evidence, by carrying successfully out clinical trials and observational studies. With a complete portfolio of professional competences, we provide clinical trial stakeholders with full support in study design, clinical operations, data management, analysis and report. With a special focus on clinical data analytics models, we satisfy the need to obtain real world evidence on investigational medicinal products and improve clinical practice by capturing a deeper knowledge about performance and safety.
Building quality, for you
As a young consulting firm, to stay on the wave with the current regulation, we have embarked on a path of structuring our activities at the highest level of compliance. This process will soon lead us to accreditation for ISO 9001 for quality, for ISO 27701, the international standard for data privacy, and for ISO 14155 for the management of research projects on medical devices.
Areas of expertise
At the service of science
STUDY DESIGN AND CLINICAL DATA CAPTURE STRATEGY
CLINICAL DATA PROTECTION AND REGULATORY COMPLIANCE
CLINICAL DATA ANALYTICS AND SCIENTIFIC PUBLISHING
Set your role in clinical research!
Did you remotize your clinical trial during COVID-19 pandemic? Or did you just stop?
Given the numerous requests received from the research stakeholders to the Clinical Trials Office and to the GCP Inspection Office, the Italian Medicines Agency (AIFA) provided indications on the management of clinical trials and the introduction of substantial trial amendments in Italy following the exceptional restrictive measures introduced by the government during the COVID-19 pandemic.
Learn today which strategies you could implement to avoid suspehending your clinical trial!
Artificial Intelligence for clinical data analysis
Classical statistics powered clinical research for decades, but machine learning and deep learning are the brand new frontier to obtain a more in-dept knowledge from data.
Big data in clinical research allow to develop artificial intelligence models, to predict outcomes, classify disease and achieve the best insights.
Soon on this website!
Power your clinical trials and speed up enrollment with Video-assisted Informed Consent
Informed consent is one of the key operations in a clinical trial, due to its paramount importance in either clinical and ethical aspects. Sometimes, administering the consent and delivering a clear and full informative to each of the study subject is time consuming.
Engage the patient and shorten the investigator’s burden with the Video-Assisted Informed Consent!