Dedicated to cosmetic manufacturers and importers in İzmir, Manisa, Aydın, Denizli, Muğla, Afyonkarahisar, Kütahya and Uşak: STE service, product safety reports, SDS and accredited laboratory testing in one place.
Each can be ordered on its own; planned together, tests, report and notifications come together in one file.
Under Türkiye's Cosmetic Products Regulation, the responsible person must have a Responsible Technical Person who checks that products comply with cosmetics legislation, GMP and related rules.
We prepare the mandatory cosmetic product safety assessment report (Annex I, Part A and B) with qualified safety assessors before your product is placed on the market.
16-section safety data sheets compliant with REACH Annex II (EU 2020/878) and CLP, in the languages of 40 countries — including UFI and PCN notification.
We organise the tests your safety assessment needs through contracted accredited laboratories and add the reports straight to your product file.
İzmir Laboratuvar is a regional project serving only companies in Türkiye's Aegean region — a team that knows the region, short lines of communication and personal follow-up.
Our services are limited to companies operating in these 8 provinces of the Aegean region.
We organise the tests your safety assessment needs through accredited partner laboratories and add the reports directly to your CPSR and PIF.
Bacteria, yeasts and moulds — the microbiological quality of each batch.
Counts the bacteria, yeasts and moulds in the product and checks for specified pathogens, showing that the product is safe to use and will not spoil.
For the microbiological quality section of the CPSR and for batch release — especially for water-based products.
Shows that the preservative system protects the product during use.
The product is deliberately inoculated with known microorganisms and their reduction is measured at set intervals, proving that the preservation protects the product throughout its use.
For water-containing and other products at microbial risk; low-risk products may be exempted after a documented risk assessment.
Confirms the product stays stable in its packaging until the end of its shelf life.
Tracks how appearance, colour, odour, pH, viscosity and weight change under different storage conditions, and whether the formula interacts with its packaging. The results support the shelf life or PAO on the label.
For every new formula or packaging change — required data for the CPSR.
Skin tolerance on volunteers or skin models — the basis for “dermatologically tested” claims.
Evaluates the risk of irritation or sensitisation, either on volunteers under dermatologist supervision or on reconstructed human skin models.
When you claim “dermatologically tested” or similar, and for products for sensitive skin, babies or the eye area.
Test plans are set per product by the safety assessor. Prices are quoted on request.
59 analyses carried out in accredited laboratories. Prices on request.
GC-MS/headspace quantification of this carcinogenic by-product of ethoxylated surfactants (SLES, PEG, polysorbates), proving it stays below the permitted trace level.
Quantifies 2-phenoxyethanol, one of the most widely used preservatives, by chromatography per Directive 96/45/EC, to verify compliance with the 1.0% limit in finished products.
Quantifies acetone in nail-polish removers and other products, for the technical file or to substantiate “acetone-free” claims.
Determines the total viable bacterial load per ISO 21149 to confirm production hygiene and product safety — a basic, mandatory step for every product file.
GC-FID determination of volatile impurities such as methanol, ethyl acetate and acetaldehyde in alcohol-based products, proving the absence of prohibited toxic impurities.
Measures the ethanol content of colognes, perfumes, toners, hand gels and hair lotions, verifying the alcohol degree declared on the label.
GC-FID/GC-MS screening for ethanol and its derivatives, used to substantiate “alcohol-free” claims on baby, eye-area and sensitive-skin products.
Quantifies aluminium compounds in deodorants, antiperspirants, sunscreens and colour cosmetics to verify compliance with safe-use limits.
Determines free ammonia in hair dyes, bleaches and nail products, to check legal limits or substantiate “ammonia-free” claims.
Quantifies anionic surfactants — the main cleansing and foaming agents in shampoos, shower gels and liquid soaps — per ISO 2271, to verify the specification.
Quantifies antimony, a risk metal that can migrate from pigments or packaging into colour cosmetics such as eyeshadow and blush.
Quantifies arsenic, a toxic element that can enter cosmetics from natural minerals, clays or water-based raw materials, against legal limits.
REACH Annex II (EU 2020/878) and CLP-compliant SDS, UFI code generation and Poison Centre Notification (PCN) via ECHA. Select your target countries to see which languages you need.
16-section safety data sheet under REACH Annex II, CLP classification, H/P statements and pictograms, kept up to date.
Unique Formula Identifier generated from your VAT number and formulation number, ready to print on the label.
Poison Centre Notification under CLP Annex VIII, submitted through the ECHA portal for every target country.
Language versions follow each country's official languages; the final set is confirmed per product.
From ÜTS to the EU, UK and US markets: all the regulatory services your products need.
STE, ÜTS, safety reports, SDS, testing or export — type your question and get an instant answer.
Talk your product through with one of our specialists and we'll define the services you need together.
Talk to the teamLet's bring STE, report and testing into one plan, with a clear timeline and quote.
Tell us about your products and the services you need; a specialist will reply with a quote and timeline.
Use the quote form or write to us directly; we'll get back to you as soon as possible.
