Thanks to local partners, Artialis is able to manage clinical studies in many countries of Central and Eastern Europe, India, Malaysia, the United States and South America.
Thanks to a large regulatory expertise and an integrated quality management system, we are able to carry out clinical studies on medical devices, food supplements and medicines. In addition, we are used to carry out validation studies of biomarkers based on in vitro diagnostic medical devices.
Our experience in biomarker analysis combined with the analysis of clinical data allows us to propose analytical methodologies adapted to the needs of each study. In addition, we have established a privileged partnership with a company specializing in the statistical analysis of our data.
Our specialization in a niche market, namely musculoskeletal disorders, allowed us to acquire a broad scientific, medical and technical expertise in clinical studies. Firstly, we propose a scientific and medical expertise in the study design with robust and innovative evaluation parameters. In addition, we offer technical expertise covering every stage of a clinical study: selection of investigators, regulatory submission, clinical documentation, monitoring, data management, statistical analysis and scientific writing.
Artialis developed its own tools to accelerate the patient recruitment and reduce the duration of a clinical study. Thanks to a well-established network of investigators and external flying nurses, we have investigating sites of trust, available and able to motivate their patients. We also performs advertising of our clinical studies using social networks, foundations, specialized websites and press campaigns.