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Clinical Trials

Performing Clinical Trials at your hospital or clinic brings several benefits:

  • Additional revenues and operating budget for the institution.

  • Professional development opportunities for clinical staff.

  • Development of overall research capabilities in a profitable format.

  • Contributing to the safe development of the next generation of medications and medical devices.

  • Increased institutional and individual prestige.


Our technology provides the following advantages to hospitals and CROs wishing to attract more clinical trials:

  • Clinical sites using our EPR system will be able to run algorithms locally to identify and cross reference patients with potential clinical trials, allowing for the pooling of potential candidates across multiple locations.

  • Our AI technology federates data – i.e. it can take medical data from multiple sites and harmonise into one data set. This allows individual hospital sites and Contract Research Organisations (CROs) to more easily participate in larger studies that span multiple sites.

  • Our Blockchain Technology provides concrete assurance regarding patient consents. Ensuring proper subject consent is absolutely fundamental to the proper conduct of clinical trials. Any type of necessary consent for any ethical or regulatory consideration can be recorded in a private blockchain as an immutable proof of the patient’s willingness. Withdrawal of consent can also be recorded at any time.


If you are interested in either hosting or conducting trials, please contact us at +352 661 684 263

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