Cosmetic Patch Test
Obtain documented skin-tolerance results from a 48-hour patch test involving ten volunteers.
What we handle
- A 48-hour in vivo cosmetic patch test involving ten volunteers.
- A signed laboratory report covering the agreed test.
What we need from you
- 40 g or ml of product, subject to laboratory acceptance.
- Full formula, product specification and intended use.
- Relevant safety information and any existing test reports.
Scope boundaries
- Sample shipping, additional tests and retesting are excluded.
- The test does not guarantee absence of reactions in all users or automatically justify hypoallergenic/efficacy claims.
From enquiry to deliverable
Confirm the product and scope
Tell us what you sell, where it will be sold and what evidence is already available. If you are unsure, contact us before ordering.
Submit the intake and pay securely
The application leads to Stripe Checkout for this exact service in EUR. Send the listed documents to info@fdabridge.com; do not send samples without instructions.
Receive the agreed work
We review document completeness, coordinate the assessment or testing and deliver the agreed report or file. Any additional scope is explained before further work.
Is this a complete clinical efficacy study?
No. It is the specified skin-tolerance patch test. Any efficacy study or wider clinical claim requires a separately agreed scope.
Official background: European Commission: EU cosmetics legislation. FDABridge is an independent private provider. Assessment, review and notification are not government approval.