Transparency Portal

Institutional and organizational information

  • Key applicable regulations

    Below we highlight key regulations that Quibim must comply with based on its operations. We are committed to upholding the highest level of compliance in all areas.


    • Regulation 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices.

    • Regulation 2016/679 of the European Parliament and of the Council of 27 April 2016 on the protection of natural persons with regard to the processing of personal data and on the free movement of such data.

    • Legislative Royal Decree 1/2010, of July 2, approving the revised text of the Spanish Companies Act.

    • Law 14/2007, of 3 July, on Biomedical Research.

  • What Quibim does?

    At Quibim, we partner with top-tier biopharma companies and healthcare institutions to apply AI techniques to medical images, extracting the latest insights into cancer and other diseases to unlock new data that can lead to prognostic or predictive models that connect research with personalized care.

    The business model is based on a platform marketed through SaaS for hospitals and value-based partnerships in life sciences that help to identify new market needs and create new algorithms. We are building an outstanding portfolio of tools for clinical use, including regulatory-cleared medical devices to extract objective and accurate information automatically.

  • Organizational structure and profiles of our leadership

Agreements entered into with public institutions and other grants

Information updated on November 15, 2023