Let’s discuss your imaging strategy.
From site qualification to imaging governance, we help sponsors reduce
variability, strengthen endpoints and improve regulatory readiness in
complex clinical studies.
Reach us by mail or by filling in the form.
Our scientific team is available to conduct a preliminary assessment of your study, offering direct consultation on:
- The definition and robustness of imaging endpoints
- Technical challenges and multicentre variability
- Centralised review strategies
- Alignment with international regulatory requirements
- Studies involving radiopharmaceuticals and clinical dosimetry
We operate as a CRO specialising in clinical imaging, with a methodological approach focused on data quality and regulatory sustainability.
Request a scientific consultationA technical discussion in the early stages of the study can prevent deviations, delays and statistical issues. We are available for:
- Preliminary protocol reviews
- Evaluation of the imaging charter
- Multicentre feasibility analysis
- Support during early-phase or pivotal studies
Talk to an imaging scientist.
Tell us about your study and we’ll route you to the right person on the team.
Via Agostino da Montefeltro 2
10134 Torino, Italy
Your enquiry is on its way.
- We review your message.
- We route the enquiry to the relevant specialist.
- That specialist contacts you directly by email.
Is your request time-sensitive? Call +39 389 945 4479 or email our team.
We reply to every enquiry, typically within one to two business days. If it’s urgent, call +39 389 945 4479.
Enquiries are handled in confidence by our scientific team. We are happy to sign an NDA before you share protocol details — just say so in your message.
Come find us in Turin
Our team works out of Toolbox Coworking in the heart of Turin, Italy.
