Streamlined machine QA for stereotactic radiosurgery. Built around structured QA workflows, ChromatiQ takes a workflow-first approach — simple, precise, and aligned with AAPM guidance.
ChromatiQ handles the full QA workflow for stereotactic radiosurgery, from film analysis to compliance reporting, in one coherent platform.
High-accuracy dose analysis from radiochromic film optimized for stereotactic radiosurgery field sizes and dose levels.
Structured QA workflows aligned with TG-178 and TG-235, so every step is documented and audit-ready.
Access QA records, results, and reports from anywhere. No local installation required — designed for modern clinical environments.
Every QA session follows a structured, guided workflow — minimizing manual steps and supporting consistent, repeatable results.
Generate clear QA reports with the measurement evidence, pass/fail status, and context needed for clinical review and record-keeping.
Multi-user access with role-based controls so physicists, technicians, and radiation oncologists each have the right level of visibility.
ChromatiQ is designed for multi-user clinical environments. Role-based access ensures that physicists, dosimetrists, and QA managers each operate within the right scope — whether at a single institution or across multiple sites.
In stereotactic radiosurgery, reliable dose measurement with sub-millimeter spatial accuracy is paramount. Steep dose gradients and small target volumes leave little room for uncertainty — every measurement must be traceable, precise, and defensible.
That's why ChromatiQ is built on proven radiochromic film methods. Film dosimetry provides the high-resolution, two-dimensional dose distributions needed to extract critical metrics — profile widths, penumbra, output factors, and isodose agreement — with the spatial fidelity that SRS demands.
ChromatiQ is designed around the key protocols governing SRS QA practice.
Guidance document for Gamma Knife dosimetry. ChromatiQ QA workflows are structured in alignment with TG-178 recommendations for SRS dose verification.
Guidance document for radiochromic film dosimetry. ChromatiQ workflows reflect TG-235 recommendations for film calibration, scanning, and analysis.
AAPM task group reports are professional guidance documents, not certifiable standards. ChromatiQ supports machine quality assurance; it is not a medical device and is not intended for patient-specific treatment planning or clinical decision-making.
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ChromatiQ is licensed per institution. Access requires an account — contact us for licensing details and trial access.