Dermatology AI for teledermatology and telemedicine platforms

A skin check patients can run before booking a paid consultation, with an informational suggestion in under a second.

Used by leading teledermatology and telehealth platforms

CE-marked Class I medical device (MDD), MDR Class IIa in progress · MHRA device registered (UK) · FDA Breakthrough Device Designation, clearance pending

What the API returns

One call, one image, one structured response. Everything below is available from the first request.

Five ranked condition suggestions per image, each with a confidence score

70+ conditions across nine dermatology categories: benign, pre-malignant, malignant, inflammatory, infectious, genodermatoses, pigmentation, hair and nail

A response in under a second

No identifiable patient data stored. Images are processed and anonymised

A standard REST call and a JSON response, with no SDK lock-in

ICD-10 reference codes alongside each result, for information only

Full white-labelling. No Autoderm branding is visible to users unless the platform chooses to show it

Where Autoderm stops

Autoderm analyses the image and returns the ranked list. Everything after that is designed by the provider:

  • Whether confidence scores are shown to users
  • Where users go for further information on a condition
  • What the next step offers: a paid consultation, a self-care pathway, or nothing at all
  • How to provide end user instructions

Autoderm reviews and confirms the compliance of the interface before deployment, so those decisions are made with the platform rather than around it.

The same analysis and interface model runs across Autoderm’s dermatology AI solutions, including dermatology AI for pharmacy and dermatology AI for virtual primary care.

What the evidence actually says

Every figure traces to a named study, with full detail on the clinical evidence page.

93%

    Top-5 suggestion accuracy

    Coachella Study 2025

3M+ API calls, 6 countries

Zero safety incidents since 2018

    Post-market surveillance, MHRA/BfArM/FDA MAUDE/ClinicalTrials.gov. Distinct from user-reported dissatisfaction (image quality), not a safety measure.

Bias evaluated across skin tones

Fitzpatrick17K bias evaluation completed across 26 conditions and FST I–VI. No systemic bias detected. Direct same-model cross-population comparisons available (Sweden FST I–II vs. Uganda FST VI on V0.1), with subsequent dataset diversification in V2.x.

    Fitzpatrick17K Bias Evaluation, 2024

How the Autoderm API integrates

A dedicated success manager guides the deployment from first call to go-live.

01

Scope and contract.

Custom pricing and contract terms, set for the platform's volume and rollout

02

Onboard and integrate.

Hands-on integration assistance builds the check into the platform

03

Launch and support.

Priority support and custom SLAs carry through go-live and beyond

Regulatory & data
protection standards

Autoderm is developed with strict adherence to European and international requirements for safe, privacy-preserving AI in healthcare.

CE Class 1 medical deviceFDA Breakthrough Device Designation badgeMHRA device notification (UK)
Learn more about our regulatory compliance

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Common questions about the teledermatology integration

No. The suggestion is informational only. It sits before the consultation, not instead of it, so users arrive with a clearer sense of what they need and clinician time goes to the cases that need it.

No. The suggestion can stand alone, or route to a consultation, a self-care pathway, or nothing at all. None of these is required by default, and Autoderm doesn’t make that decision.

No identifiable patient data is stored. Images are processed and anonymised, and the service is GDPR-compliant by design.

Pricing is scoped to the deployment, based on API volume and the contract terms the platform needs. There’s no fixed rate card at this tier; the specifics are set with a dedicated success manager as part of onboarding.