What is the ScanSkinAI Cancer Flag Module?+
The Cancer Flag Module is a non-diagnostic AI screening tool that assesses a lesion from an ordinary clinical photograph and flags whether it warrants closer attention from a clinician. It identifies patterns consistent with basal cell carcinoma, melanoma, squamous cell carcinoma, and benign or other lesions, and communicates the result as a triage signal rather than a diagnosis.
What AI model architecture powers the Cancer Flag Module?+
The visual backbone is a DINOv2-Large vision transformer (ViT-L/14) operating at native 518×518 resolution, chosen for its self-supervised representation quality on natural images and its ability to preserve fine lesion detail. A second, bounded language layer sits on top of the classifier to communicate the result responsibly without ever issuing a diagnosis.
Is the model validated across different skin tones?+
Yes. Performance is evaluated across Fitzpatrick skin types I through VI, using both an internal held-out set and an independent dermatologist audit of production scans. Cross-tone validation is treated as a first-class design requirement, not a post-hoc check — most publicly available datasets skew heavily toward lighter phenotypes, and the paper documents how that gap is addressed.
How does the model handle rare cancers like melanoma?+
Melanoma and squamous cell carcinoma are rare in any real-world dataset, and missing them is the costliest error a screening tool can make. The paper details the class-imbalance strategy, weighted sampling, and a progressive three-phase fine-tuning regimen used to keep sensitivity high on these minority classes without inflating false positives on benign lesions.
Does ScanSkinAI diagnose skin cancer?+
No. The Cancer Flag Module is a non-diagnostic screening and triage aid. It supports earlier attention and clinician review and does not replace dermoscopy, biopsy, histopathology, or in-person examination. Any concerning, changing, bleeding, or non-healing skin change should be assessed by a qualified clinician.
What regulatory and quality standards apply?+
The module is developed under an ISO 13485 medical-device quality management system and an ISO 27001 information-security framework. It is aligned with UKCA Class I and EU MDR requirements as software as a medical device (SaMD) positioned for non-diagnostic screening.
How is the model made explainable?+
Grad-CAM and SHAP are used to make the model's attention inspectable, so clinicians and reviewers can see which regions of a lesion drove a prediction rather than trust the output blindly. The paper also sets out the full development and validation lifecycle and our roadmap for continued validation.
How can I cite this whitepaper?+
Cite as: Ivy AI Solutions Limited (2026). ScanSkinAI Cancer Flag Module: Training Methodology, Model Development, and Robustness Evaluation. Zenodo. https://doi.org/10.5281/zenodo.21225287. The DOI resolves to the archived version of record.