Make-up products must give the consumer a high degree of safety and be very competitive on the market. It is therefore important to design testing protocols that allow to meet all the necessary requirements.
Abich – Lifeanalytics, the Group’s Competence Center for Pharma and Cosmetics industries, offers the full range of tests necessary to ensure the safety and efficacy of your make-up products. Our highly-specialised team will help you develop an accurate and repeatable testing protocol that meets your needs.
The clinical test is designed to be applied to eye contour cosmetics or products that require to confirm the compatibility with the periocular mucosa in normal usage conditions with the purpose of substantiating the claim “Ophthalmologically tested” according to Guidelines to Commission Regulation (EU) No 655/2013.
An ophthalmology specialist will inspect the target area, and especially the eyelids, before the application using a fissure lamp, in order to confirm the absence of swelling, hyperemia, dryness or desquamation. The inspection also rules off alterations of the eyelashes.
In the eye itself, the integrity of the cornea and conjunctiva, the absence of hyperemia, and signs of conjunctival or tarsal irritation are verified. Finally, the absence of qualitative and quantitative alterations in the tear film.
The specialist then evaluates and scores erythemal response, tearing, edema and dryness after the product has been used for 30 minutes, 2 days and 30 days to quantify possible alterations induced by the sample.
The volunteers also provide subjective evaluations of itching, burning, stinging or foreign body response feeling, and/or sight clouding, at the same endpoints, using the VAS (Visual Analogical Scale) score system.
The clinical test is designed to be applied to makeup and lipsticks with the purpose of substantiating the claim “Long lasting” according to Guidelines to Commission Regulation (EU) No 655/2013.
Instrumental colorimetric evaluation: the evaluation can only be performed on pigmented products and is not applicable to transparent cosmetics. Clinical evaluation: digital imaging of the treated area at T=0 and after X hours from the application of the product. The duration of the treatment is agreed upon with the sponsor before the test.
The test is designed to be applied to makeup and lipsticks with the purpose of substantiating the claim “No transfer” according to Guidelines to Commission Regulation (EU) No 655/2013.
Digital images of the treated area are captured immediately after application of the product and after contact with test items. Depending on the type of product testing, contact items include skin, paper cups, glass cups, napkins, white clothes.
The test is designed to be applied to cosmetic products with the purpose of substantiating the claim “Sensitizing metals below risk threshold” according to current regulations.
Mineralization/high pressure microwave dissolution and determination through ICP-OES.
The in vitro test is designed to be applied to raw materials and finished products with the purpose of substantiating the claim “Anti-pollution” according to proprietary method.
In vitro test for the evaluation of the protective effect against air pollution. The purpose of this test is to evaluate the efficacy of the sample in reducing ROS release in response to a mix of heavy metals and atmospheric dust particulate in a skin-derived cell model.
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