Kanteron Platform

Kanteron Platform is a patient-centric enterprise clinical content platform developed by Kanteron Systems. It integrates medical imaging, digital pathology, clinical genomics, pharmacogenomics, and biosensor data into a single environment, designed for healthcare organisations seeking to consolidate disparate clinical data sources. The platform is built around on-site or private cloud deployment, using open standards and open-source components, and is accessible via HTML5 web browser on any device or operating system.

The platform is structured as a set of specific workflow modules — covering radiology, pathology, genomics, pharmacogenomics, analytics, and telemedicine — rather than isolated silos. It supports a 360-degree view of the patient by bringing together all modalities, images, sequences, results, reports, and prior records in one place.

Data Management Architecture

• Ingest and store: data can be kept on-site or in a private cloud, without requiring data to leave the hospital
• Integrate: uses open-source components and established standards including DICOM, HL7, FHIR, WADO, XML-RPC, and LDAP
• Analyze: supports AI/ML models and third-party algorithms
• Visualize and report: zero-footprint (ZFP) browser-based viewing and synoptic reporting via web browser

Radiology Module (PACS-RIS-VNA)

• Multi-center scheduling with instructions and consent management
• Radiologist worklist with voice recognition integration, reporting tools, and workstation support
• Technologist worklist with filtering, modification, and worklist server capabilities
• Transcriptionist module
• Access to priors and patient records
• Synoptic reporting
• Patient and referring physician report portal
• Zero-footprint HTML5 browser-based DICOM viewer
• PACS management console with MMWLS, backup, auditing, logging, MPPS, GP, and GPPPS support

Digital Pathology Module

• Vendor-neutral Dicomizer compatible with any scanner
• Case and order management
• Whole slide image (WSI) zero-footprint browser-based viewer
• Synoptic reporting with templates and voice recognition integration
• Remote upload of WSI
• Integration with EHR and LIS systems

Clinical Genomics Module

• Integration of genomic and genetic data into EMR, HIS, and LIMS for on-site and external laboratories, following HL7 FHIR Genomic specifications
• Real-time navigation through genomic features across somatic and germline variant data
• Automated workflow covering import of NGS files (FASTQ, BAM, VCF, GFF, BED), QA checking, processing, visualisation, and browser-based report generation
• Clinical interpretation tools including exploration and evaluation of prioritised and annotated variants, variant filtering by region, functional consequence, VAF, and other parameters
• Curation and clinical annotation for historical review and on-premise genomic knowledgebase creation
• Integration with eCRF or clinical data management (CDM) systems for clinical trials

Pharmacogenomics Module

• Incorporates drug-gene interaction data from major pharmacogenomic databases including PharmGKB, CGI, DGIdb, and OpenTargets
• Allows query refinement by gene family, interaction type, drug class, and other parameters
• Integrates known drug-gene interactions and druggable gene data with patient genetic background into the EMR
• Supports configurable warning levels in the EHR for drug/genomic-variant interactions
• Supports addition and curation of custom data, and annotation of genes of interest with respect to drug-gene interactions and druggability
• Aimed at adverse medication event prevention and precision medicine application at the point of care

Analytics and AI/ML Module

• Flexible AI framework allowing users to select the dataset and algorithm that best fits their use case and apply it to relevant medical images
• Includes a prostate cancer training set as a starting point, with the ability to select from a list of available models and their descriptions
• Developed in collaboration with the Medical Informatics Laboratory at Queen's University and the Surgical Planning Laboratory at Harvard Medical School
• Supports AI-assisted second opinion for radiologists alongside standard image viewing and reporting

Telemedicine and Collaboration Module

• Secure videoconference, shared screen, text, and audio communication
• Supports multidisciplinary team (MDT) collaboration and tumour boards
• Enables telemedicine, teleradiology, and telepathology workflows
• Additional features include dashboard, data auditing, logging, cloud security ("SPLIT"), and direct transfer

The platform holds a European CE mark and is manufactured under Medical Device Manufacturer License (Spain) number 7506-PS. It is certified to EN ISO 9001:2008 by Bureau Veritas and to ISO 13485. In the United States, the software is excluded from the definition of a "device" under Section 3060 of the 21st Century Cures Act. The platform is headquartered in Valencia, Spain.