Published June 9 2026
At AIRS Medical, we believe artificial intelligence should support healthcare professionals, improve operational efficiency, and help healthcare organizations deliver better patient experiences while maintaining high standards of safety, transparency, privacy, security, and accountability.
Our AI technologies are designed to assist radiologists, technologists, and healthcare organizations by enhancing MRI workflows and image quality while preserving the critical role of clinician expertise and decision-making.
AIRS Medical is committed to the responsible development, deployment, and use of AI technologies through principles focused on clinical responsibility, transparency, privacy, security, fairness, and continuous improvement.
AIRS Medical AI technologies are intended to support qualified healthcare professionals and are not designed to independently diagnose, replace clinical interpretation, or substitute professional medical judgment.
Clinical decisions remain under the supervision and responsibility of licensed medical professionals.
AIRS Medical develops and maintains AI technologies within structured quality, testing, validation, governance, and risk management processes intended to support safe and reliable performance in clinical environments.
Where applicable, AIRS Medical products may be subject to regulatory review, clearance, approval, or market-specific compliance requirements depending on intended use and jurisdiction.
AIRS Medical is committed to ongoing validation, monitoring, and performance evaluation to support responsible deployment in healthcare environments.
We strive to provide clear and accessible information regarding the intended use, capabilities, operational considerations, and limitations of our AI technologies so healthcare organizations can make informed decisions regarding implementation and use.
Where appropriate, AIRS Medical aims to provide users with meaningful information regarding system functionality and expected use within clinical workflows.
Where our products generate or modify content (for example, enhanced or reconstructed images and AI-generated reports), AIRS Medical implements measures, where applicable, so that such outputs are identifiable as AI-generated or AI-modified, consistent with applicable transparency requirements and the authoritative information provided in each product’s Instructions For Use.
AIRS Medical applies industry-standard privacy and data protection practices designed to protect customer and patient information and support compliance with applicable healthcare, privacy, and data protection requirements.
AIRS Medical does not use customer or patient data to train AI models without appropriate authorization, contractual agreement, customer consent where required, or other applicable legal basis.
Where applicable, safeguards are implemented to support responsible handling, storage, transmission, retention, and processing of customer and patient data.
AIRS Medical implements technical, administrative, and organizational safeguards designed to protect systems, infrastructure, products, and customer environments from unauthorized access, misuse, alteration, disclosure, or destruction.
For further details on how AIRS Medical processes personal data, please refer to our Privacy Policy.
AIRS Medical recognizes that AI systems may present limitations or performance variability across clinical environments, imaging protocols, equipment configurations, and patient populations.
We are committed to ongoing evaluation, monitoring, testing, and improvement intended to support fairness, reliability, consistency, and responsible deployment of AI technologies.
AIRS Medical seeks to identify and mitigate potential risks, unintended outcomes, operational limitations, and sources of bias as part of its responsible AI practices.
AIRS Medical monitors AI-enabled technologies throughout their lifecycle, including performance, reliability, security, and potential changes that may affect intended use or clinical performance.
Material updates to AI-enabled technologies are reviewed through appropriate quality, validation, risk management, security, and regulatory assessment processes before release.
AIRS Medical considers data quality, clinical relevance, imaging protocols, scanner environments, and performance variability as part of AI development, validation, deployment, and monitoring activities.
Our responsible AI approach is informed by recognized AI risk management practices, including governance, risk assessment, measurement, monitoring, and mitigation.
AIRS Medical uses AI technologies to support MRI workflow enhancement, image processing, operational efficiency, and product innovation.
Depending on the product and deployment environment, AI capabilities may include:
Where a listed capability forms part of a regulated medical device, it is provided only within that product’s cleared or approved intended use in the applicable market.
AIRS Medical may also utilize carefully evaluated third-party AI technologies to support internal business operations and product development activities. Where applicable, safeguards are implemented to help protect customer and patient data and support responsible use.
AIRS Medical continuously evaluates its AI technologies, internal processes, governance practices, and security controls to support responsible innovation and alignment with applicable laws, regulations, contractual obligations, and industry expectations.
Our approach to AI governance includes internal review processes, risk assessment, security oversight, employee education, and ongoing monitoring intended to support the safe and responsible deployment of AI technologies.
AIRS Medical encourages customers and users to report unexpected, unsafe, inaccurate, or potentially harmful AI-related behavior so concerns can be reviewed, investigated, and addressed appropriately.
If you have questions regarding AIRS Medical’s use of AI technologies or would like additional information, please contact us at: [email protected].
For questions regarding privacy or data protection, please contact: [email protected]
This AI Transparency Statement may be updated periodically as AIRS Medical’s technologies, products, regulatory obligations, compliance requirements, and AI governance practices evolve.
This statement provides general information about AIRS Medical’s approach to AI and does not describe the regulatory status, intended purpose, indications, or performance of any specific product. For each product, the authoritative information is set out in its Instructions for Use (IFU), labeling, and the regulatory clearances or certifications applicable in the relevant market. This statement is provided for informational purposes only and does not create any representation, warranty, or legally binding commitment. Product-specific terms are governed by the applicable agreements and product documentation.