Clinical Studies

Intelligent clinical studies.
Integrated with your go-to-market model.

At Devicia we work exclusively with clinical studies for medical devices. Why? Based on our experience, device clients are often very different from pharmaceutical companies and require another set of services and competencies. Focusing our efforts, means we can cater specifically to the device client. Bringing the product in the hands of the consumers as soon – and safely – as possible.

  • Helping you help
    those who need it most

    Our aim is to provide services to enable your customers to benefit from your products as quickly and safely as possible. When working with us, you get access to a team specialized exclusively in clinical trials for medical devices. Furthermore, our quality control system, which is based on ISO 14155, is specifically tailored to the requirements of medical device clinical studies. When designing clinical studies, we always consider the reimbursement landscape in order to make the product available to as many consumers as possible.

  • Pre- and post-market
    clinical study management

    We provide a full set of services to help you generate clinical data, before and after CE mark. When working with us, our team helps you effectively integrate your clinical studies into your go-to-market model. That involves all kinds of studies such as first in human studies, feasibility or pilot studies, randomized controlled trials and registries.

Our clinical study services

Clinical Investigation Plan (CIP)
Ethics Committee Applications / Competent Authority Application
Patient Recruitment
Development Case Report Form (CRF)
Development Patient information and informed consent forms
Site visits, project management and monitoring
Statistics and data management
Want to know more about our services
for medical device clinical studies?
Contact Us