The Devicia Difference

An ambitious approach.
For a precise outcome.

For almost ten years, we have helped medical device clients generate clinical data for regulatory approvals, reimbursement and marketing purposes. We simplify clinical studies and reduce time to market.

  • One point of contact
    throughout your project

    With Devicia you will have a professional client leader throughout your project, who safeguards the execution and predictability of your development milestones.

  • Medical device-specific
    quality management system

    Our quality system is tailored to the Medical Device Directives and ISO 14155, and it is audited by Symbioteq.

  • Local knowledge
    and global access

    Through our global network of accredited subcontractors you get assistance in regional work, such as monitoring and local regulatory submissions. All our subcontractors are trained on our standard operating procedures (SOPs). Currently, we are managing a number of multi-site studies – ranging from 15 to 200 patients, at up to 15 simultaneous locations.

  • Study management
    model and tools

    Building on our unique experience as a device-only clinical research organization (CRO), we work according to a tailored set of tools to facilitate consistency, compliance and predictability for all studies. We support your studies from start-up, to site activation, patient enrollment and data review. Moreover, our data management tools are tailored for device development to support efficient, secure and timely execution and accurate metrics to both sites and sponsors.

What difference can we do for you? Contact us for more information