SeeTreat's ART.1 is now CE Marked under EU MDR - Bringing Adaptive Radiotherapy to Every Clinic
Tuesday, November 11, 2025
SeeTreat announced today that its offline adaptive radiotherapy software, ART.1, has received CE Mark certification under the European Union Medical Device Regulation and is now available for clinical use across the European Union.
SYDNEY, Nov. 6, 2025 /PRNewswire-PRWeb/ -- SeeTreat announced today that its offline adaptive radiotherapy software, ART.1, has received CE Mark certification under the European Union Medical Device Regulation and is now available for clinical use across the European Union.
ART.1 software provides objective, evidence-based decision support for clinical teams to adapt (i.e. modify) radiotherapy treatment to match each individual patient's changing anatomy throughout their treatment. By automatically analysing delivered radiation dose and anatomical changes from daily imaging, ART.1 enables clinical teams to evaluate in minutes whether a patient's treatment should be adjusted or continue as planned, a process that can otherwise take several hours or even days.
"ART.1 changes what's possible in adaptive radiotherapy. It gives clinicians continuous visibility into how treatment is evolving for each patient, bridging the gap between planning and real-world delivery in a way that's been missing until now," said Dr. Jarad Martin, practicing radiation oncologist (MBChB BSc PhD DMed FRANZCR GAustMS), SeeTreat CMO.
What ART.1 Brings to Clinical Teams Across Europe
Timely access to radiotherapy remains one of Europe's most pressing cancer care challenges. The European Cancer Organisation (ECO) reports that every four-week delay in treatment initiation increases mortality by up to 13 percent*, underscoring the urgent need to optimise every step of the treatment pathway from planning to delivery.
ART.1 addresses this gap within the treatment phase, helping radiotherapy teams deliver the latest in personalised adaptive-quality care more efficiently without adding hardware, staff, or workflow burden.
-- Turns daily imaging into objective insight: automatically calculates
delivered dose and anatomical changes from daily CBCTs to compare each
fraction against the planned treatment.
-- Focuses clinician time where it's needed most: continuously analyses
treatment data in the background and flags deviating cases prioritised
for review.
-- Streamlines adaptive workflow: provides quantified analytics from
detection to decision support for every structure, every fraction, and
every patient.
-- Integrates with existing systems: requires no hardware upgrades,
workflow disruption, or additional staffing.
-- Expands access to adaptive radiotherapy: brings objective, data-driven
decision support to both major cancer centres and community clinics,
enabling more patients to start and stay on treatment without delay.
"Innovation in cancer care doesn't have to come only from the biggest players," said Dr. Trang Nguyen, SeeTreat CEO and Founder. "We started SeeTreat to give every clinic, large or small, the same opportunity to deliver truly personalised care. Smart, focused innovation can have a global impact and ART.1 is our first step in a pipeline of products for improving oncology treatment precision on a global scale."
About SeeTreat
SeeTreat is an Australian medical technology company focused on making adaptive radiotherapy safer, faster, and more accessible. Founded in 2023 by Dr. Trang Nguyen and Prof. Paul Keall, SeeTreat enables equitable access to precision cancer treatment, with the vision to reduce the burden of cancer worldwide. The company builds intelligent software that automates the most difficult parts of the adaptive workflow--helping more clinics deliver adaptive-quality care, every day.
Regulatory status: ART.1 is UKCA Marked and CE Marked and available for clinical use in the UK and EU. It is for Research Use Only (RUO) in all other markets. FDA 510(k) clearance is pending.
*European Cancer Organisation. Getting There on Time: Securing the Future of Cancer Care in Europe. 2023. https://www.europeancancer.org
Media Contact
Michelle Joiner, SeeTreat, 1 6789384163, michelle@g3medicalmarketing.com, https://www.seetreatmedical.com/
View original content to download multimedia:https://www.prweb.com/releases/seetreats-art1-is-now-ce-marked-under-eu-mdr--bringing-adaptive-radiotherapy-to-every-clinic-302607313.html
SOURCE SeeTreat
|
|
|
|
|
 |
Energy Toolbase Launches Energy Storage Partnership with Sungrow to Support PowerStack 255CS and PowerTitan 2.0 | Jan 22, 2026
|
|
RS now offers Phoenix Contact's pioneering new NearFi technology | Jan 22, 2026
|
|
MetaOptics to Showcase Five Breakthrough Metalens-Powered Products at CES 2026 | Jan 22, 2026
|
|
Fresco Raises EUR15m Series C to Power the Future of AI-Driven Cooking and the Connected Kitchen Ecosystem | Jan 22, 2026
|
|
No Assembly Required: Barrett Distribution Centers Powers Maxwood Furniture's West Coast DTC Expansion | Jan 22, 2026
|
|
SCAILIUM Debuts "AI Production Layer" to Overcome GPU Starvation and Slash AI Energy Waste | Jan 22, 2026
|
|
Einride and IonQ Partnership Uses Quantum Computing to Optimize the Logistics of Electric and Autonomous Freight | Jan 22, 2026
|
|
Hesai Recognized as the Only Lidar Company on Morgan Stanley's "Humanoid Tech 25" of Global Robotics Leaders | Jan 22, 2026
|
|
Daikin Applied Invests $163M in Advanced R&D Test Lab to Bolster HVAC Innovation for Data Centers and Beyond | Jan 22, 2026
|
|
Lumana Surpasses 50,000 Cameras, Cementing Its Leadership in AI Video Surveillance | Jan 22, 2026
|
|
|
