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Definition

What the assessment covers

The study may use an open, semi-occlusive or occlusive patch protocol, or a supervised use test, depending on the question and the prior safety review. These approaches expose skin differently and cannot be treated as interchangeable. Recruitment criteria, application site, exposure conditions and observation points should be specified in advance.

A dermatologist evaluates signs such as redness and dryness alongside participant reports of stinging, burning or itching. The report should identify the tested formula, participant characteristics, protocol deviations, adverse events and the basis for the medical conclusion. Where instrumental measurements are included, they answer separate, predefined questions rather than substituting for clinical observations.

Applications

Using the findings

The deliverable is a study report with tolerance findings and a qualified interpretation for the tested population and conditions. Request a clear distinction between observations, the investigator’s opinion and any proposed claim wording. A sensitive-skin claim requires a study population and endpoints suited to that claim.

Dermatologist-tested describes testing, not a guarantee that nobody will react, a dermatologist recommendation or proof of product efficacy. This assessment does not automatically replace a jurisdiction-specific cosmetic safety assessment. Results can inform formulation changes, instructions for use or further investigation; any revised formula may need its own supporting evidence.

Exploration
Learn more about Human Tolerance Testing

Assess cosmetic tolerance in human participants through supervised patch or use studies, with observations and conclusions tied to a defined protocol. Explore another Human Tolerance Testing page on cosmetic-labs.com.

Ophthalmologist-Supervised Tolerance Testing

Assess eye-area cosmetic tolerance in a human-use study under ophthalmologist supervision, recording ocular signs and participant-reported symptoms.

Repeat-insult patch (HRIPT)

Assess sensitisation potential with a defined human repeated-insult patch-test protocol, clinical supervision and interpretation of observed reactions.

Non-Comedogenic Claim Testing

Assess comedone formation in a defined human product-use study, with observations supporting a scoped non-comedogenic claim for the tested conditions.

Dermatologist-supervised Tolerance Assessment

Assess cosmetic skin tolerance under dermatologist supervision, with a defined study protocol and a report interpreting observed reactions.

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What does “Verified” mean?

Verified means the claimant’s company affiliation was checked.

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