Thanks to our consultancy technique, as well as the multidisciplinary nature of our team, we already stem as a benchmark in the management of clinical trials. We assist our clients in every step: from the regulatory start-up phase, including submission and approval of the study, to project management, data management and statistics.
Clinical Research
Line Activation
Regulatory Approvals
Manufacturing
Distribution
Logistica
Commissioning & Qualification
Logistica
Maintenance & Engineering
The flexibility of our team and the high modularity of our services allow us to assess the most suitable and customized solution based exclusively on the client’s needs. The final objective is to guarantee total compliance with the client’s expectations in terms of quality, time and costs. Multidisciplinarity, efficiency and reactivity are only a few values that distinguish us from our competitors.
Our CRO supports pharmaceutical, biomedical, biotechnology companies, as well as laboratories and research organizations, both on a national and international scale. We operate and monitor the development of interventional and observational clinical studies. Specifically, we offer support in the following areas:
FAQs
Of course, JSB will take charge of an entire study or even just a part of it, thanks to the flexibility of its consultancy model and a targeted approach to client facilitation.
It does. Also thanks to a team composed by project managers of various seniorities, JSB can provide its clients with a complete supervision of clinical studies entrusted to others. It can be implemented through a team specifically dedicated to the clients, both on a regular basis and via consultancy packages.
Thanks to the work of its software developers team, JSB launched “Contrappunto eCRF”, which gives our customers extreme flexibility in system customization and guarantees an immediate response to every necessity.
