Clinical use case
We match the model to the clinical question, protocol and output the radiologist needs. The department’s needs are the starting point.
We are developing a platform that gives a department access to AI models from several vendors through a single PACS/RIS connection. The model is matched to the clinical use case, while integration, billing and support stay with one partner.
Model choice
One integration
Shared billing
One point of support
01Why a platform
Every model bought separately means a separate integration, a separate contract, separate support and separate billing. The platform brings these together and leaves the choice of tool with the department.
A model can be replaced by another, or two can run in parallel and be compared on the same material.
A model change reuses the existing PACS/RIS connection. We verify the new model's compatibility and how its result is presented.
Models covered by the service are billed together. The facility sees the cost of its whole AI portfolio in one place instead of settling separately with each vendor.
Tickets, integration and escalation sit with QuantumMed. The facility does not coordinate several vendors to establish who handles a problem.
The freedom of choice concerns the model vendor within the platform. We do not promise migrating the integration away from QuantumMed.
02Workflow
Changing the model reuses the same PACS/RIS connection. Model compatibility and result presentation must be verified.
The radiologist works in their own environment. The platform routes the study to the selected model and the result returns to the department's workflow. Every stage has execution conditions and error handling.
Workflow
The team is notified when an analysis was not performed or the model vendor is unavailable.
Orthopaedics
Angles and distances prepared for the radiologist to review.
Lungs
Areas flagged for attention when reporting the study.
Neuro-oncology
Perfusion parameters shown alongside the anatomical image.
03Model selection
We are building a portfolio around the needs of the department. Selection considers the model’s intended purpose, the vendor’s documentation, data processing conditions and review of the output in the radiologist’s environment.
We match the model to the clinical question, protocol and output the radiologist needs. The department’s needs are the starting point.
We check the CE marking, intended purpose and vendor documentation for the specific model. QuantumMed does not certify models.
Before a pilot we agree the data scope, processing location, responsibilities and rules for returning the result.
We agree the evaluation criteria and material with the team. We check the completeness of the result, its readability in PACS/RIS and exception handling.
05The next step
For a first conversation we need one study type, what the team needs and which PACS/RIS is in place. Together we will define which result is worth checking, which conditions must be met and who should take part in the assessment.
info@quantummed.euYou can email us to request a short scope overview or sources for a discussion of regulations.
Request a scope overviewRequest sources: GDPR and EHDS06Team
QuantumMed sp. z o.o. is a Polish company founded by Sylwester Cyrwus and Krzysztof Bokiej. We connect discussions about applications with responsibility for the technical scope.

CEO and co-founder
Leads conversations about healthcare organisations, technology use cases and collaboration. Connects organisational needs with a practical scope of work.
CTO and co-founder
Responsible for architecture and technical evaluation. Defines integration boundaries, dependencies and the evidence needed to establish how a solution works.