Home / Pathology / Proscia Concentriq
Proscia (Philadelphia, US)Proscia Concentriq
American platform for digital pathology, from research to primary diagnosis. In the Netherlands chosen by Pathologie Friesland and LabPON.

- Provider based outside the EU
- Data in the EU according to the provider
- Publishes certification/GDPR safeguards
Last checked: 9 October 2026 · How we check
Is this your tool? Fill in missing detailsWhat it does
Connects to 230+ third-party AI apps
Two-way link with LIS (e.g. Epic Beaker)
Cloud deployment (AWS)
Biomarker research and clinical trialsComparable in pathology
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Visiopharmon requestplatform with its own AI and third-party AI; ISO 27001, ISO 13485 and SOC 2 Type II. Concentriq AP-Dx carries CE marking under the IVDR for primary diagnostics. Pathologie Friesland runs it on AWS. US provider: confirm an EU region and a data processing agreement. Many tools build on a large model from, for example, OpenAI or Anthropic. If in doubt, ask for the data processing agreement: it states where your data goes.
Questions about Proscia Concentriq
- Which AI model does Proscia Concentriq use?
- The maker of Proscia Concentriq does not disclose which AI model sits underneath. Platform with in-house AI and third-party AI; ISO 27001, ISO 13485 and SOC 2 Type II. Concentriq AP-Dx is CE-marked under the IVDR for primary diagnostics. Pathologie Friesland runs it on AWS. US provider: record the EU region and a data processing agreement.
- How much does Proscia Concentriq cost?
- on request. Check the current price on the provider's website; rates change often.
- Who is Proscia Concentriq for?
- Proscia Concentriq is aimed at pathology. It supports work such as digitising and managing tissue slides in an image management system (scanners, LIMS, archive), detecting and grading cancer on H&E slides (e.g. Gleason score, mitotic count, tumour size), and counting and quantifying biomarkers in IHC staining (HER2, ER/PR, Ki-67, PD-L1).
- What should I watch out for with AI in pathology?
- You process special category personal data (health) and sometimes data for genetic research. Software for diagnostic use is an in vitro diagnostic medical device: check whether the algorithm is CE-marked under the IVDR for your exact application and tissue type. Many apps are 'research use only'. Choose providers with ISO 27001 and ISO 13485, a data processing agreement and clear data location (EU hosting or on-premise). Also ask whether your slides are used to train models. Under the EU AI Act, medical AI falling under the IVDR is classed as high-risk. Validate every algorithm locally on your own scanner and stains before using it in routine practice.
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