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Beyond the grading panel: objective skin assessment with VivoSight OCT

Cosmetic product development has long relied on expert grading panels, consumer self-assessment, and photography as the primary tools for measuring treatment effects. These methods have served the industry, but they carry inherent limitations: subjectivity between assessors, sensitivity to lighting and angle, and the fundamental inability to capture structural changes beneath the skin surface.

VivoSight OCT addresses all three. It provides fast, non-invasive, objective skin assessment.  Three-dimensional imaging of skin structure and microvasculature — and, through automated analysis software, delivers quantitative metrics that are repeatable across time points and reproducible across sites. With an imaging depth of more than 1mm and a 6×6mm field of view, VivoSight captures the full depth of the dermis and a meaningful skin area in a single 15-second scan. For R&D teams and regulatory affairs managers building the objective evidence base behind product claims, that combination is genuinely difficult to replicate by other non-invasive means.

OCT dermal brightness measurement on sun exposed skin

Leading Endpoint: Dermal Brightness as a Collagen proxy

Dermal brightness — the OCT signal intensity within the dermis — is the most clinically and commercially significant measurement VivoSight OCT enables for cosmetics research. Organised, intact dermal collagen produces a characteristic high-signal pattern on VivoSight OCT scans. As collagen degrades under UV exposure, intrinsic ageing, or inflammatory processes, this signal changes in measurable, quantifiable ways.

The result is a non-invasive, in vivo proxy for collagen content and organisation — one of the primary targets of anti-ageing and skin repair interventions — obtainable without biopsy, in a 15-second scan, and trackable longitudinally within the same subject. No other commercially available non-invasive imaging system with comparable imaging depth and field of view currently offers this capability.

This makes dermal brightness an endpoint of direct relevance to both internal R&D decision-making and external claims substantiation: it is quantitative, repeatable, and grounded in a peer-reviewed methodology established across more than 50 published studies using VivoSight OCT.

Why this matters for claims and regulatory submissions

With VivoSight OCT-derived metrics — particularly where the measurement protocol is standardised, the study is appropriately powered, and the results are peer-reviewed — represent a credible, defensible evidence base for claims substantiation. Quantitative outputs are statistician-ready and directly comparable across time points, without the variability inherent in expert grading.