Contract cosmetics & dermocosmetics manufacturing · Ankara, Türkiye
We manufacture your brand, end to end.
From concept through R&D and formulation, GMP-compliant production, registration and dispatch — the entire process runs under one roof. You grow the brand; we carry the manufacturing, the regulation and the quality.
- m² enclosed production area
- 4,000m² enclosed production areaAnkara Anatolian OIZ
- product categories
- 9product categoriesCare to dermocosmetics
- end-to-end services
- 10end-to-end servicesFormula to registration
- ISO 22716 compliant production
- GMPISO 22716 compliant productionCertified quality system
Ways of working
Four manufacturing models, matched to where your brand is
Launch fast with a proven formula, or develop something bespoke from scratch. We identify the right model with you in the first conversation.
Contract Manufacturing
The formula is yours, or developed exclusively for you; production, filling and regulatory sit with us.
ExplorePrivate Label
Choose from our tested formula library and reach market under your own brand, fast.
ExploreDermocosmetics
Active-led scientific formulations, backed by efficacy and stability testing.
ExploreOEM / ODM
Our R&D team develops the product from market insight; you sell it under your own brand.
Explore
Product categories
Manufacturing capability across nine categories
From hair care to oral care, sun protection to dermocosmetics — a broad category range that lets you build your entire product line with a single supplier.
Concept to shelf
We don't just manufacture — we make your brand legally real.
Most manufacturers hand you the product and leave the rest to you. We also establish your brand's legal existence: responsible technical person, product tracking registration, trademark filing, product safety reporting. No separate regulatory consultancy needed.
Concept-to-Shelf programmeHow we work
Seven steps from concept to shelf
We don't hide the process. You know what each stage is and how long it takes from the outset — so you can plan a launch calendar that holds.
| Step | Stage | What happens | Duration |
|---|---|---|---|
| 01 | Brief & feasibility | We align on concept, audience, target shelf price and volume. The technical team returns a feasibility read. | 2–5 days |
| 02 | Formulation development | R&D develops the formula — or adapts an existing one — to the target efficacy, texture and ingredient profile. | 2–4 weeks |
| 03 | Sample & revision | A lab sample is produced, evaluated and revised until it is signed off. | 1–3 weeks |
| 04 | Stability & safety testing | Stability, microbiology and packaging compatibility testing; the product safety report is prepared. | 4–12 weeks |
| 05 | Registration & notification | Ministry notification, ÜTS registration, responsible person assignment and all required filings are completed. | 2–4 weeks |
| 06 | Production & filling | The approved formula goes into series production under GMP conditions, then filling and packaging. | 2–4 weeks |
| 07 | Quality control & dispatch | Batch quality control, certificate of analysis and dispatch — including export documentation where needed. | 3–7 days |
Durations are typical; they vary with formula complexity, packaging lead times and test outcomes.
See the process in detailFacility
4,000 m² of enclosed production area in the Ankara Anatolian OIZ
Everything runs under one roof, from raw material intake to dispatch. A shorter supplier chain means both lead time and accountability sit in one place.
- Raw material intake and quarantine
- Every batch arrives with a certificate of analysis and is held apart until released.
- Mixing and homogenisation
- Separate lines for emulsion, gel and surfactant systems, with batch-level records.
- Clean-room filling
- Filling into tubes, bottles, jars and airless packs, with in-line weight control.
- R&D laboratory
- Formulation development, sampling and revision, cycling until you approve.
- Quality control
- pH, viscosity, microbiology and stability testing; product safety report file.
- Warehouse and dispatch
- Finished goods and packaging stock; domestic and export shipment preparation.
Quality certification
Quality is not a claim — it is certified
Our production standard is documented through independent audit. We share current copies of each certificate during the quotation process.
| Standard | Scope | What it certifies |
|---|---|---|
| ISO 22716 | Cosmetics Good Manufacturing Practices | Certifies that the entire chain — from raw material intake to dispatch — runs to the international cosmetic GMP standard. |
| ISO 9001 | Quality Management System | Demonstrates that processes are defined, measurable and managed under a continuous-improvement quality system. |
| ISO 14001 | Environmental Management System | Certifies that waste, water and energy management are run systematically to reduce environmental impact. |
| ISO 45001 | Occupational Health & Safety | Shows that occupational health and safety risks on the production floor are managed under a defined system. |
Frequently asked questions
What brands ask most about contract manufacturing
If your question isn't here, ask us directly — we respond to quote requests within 24 hours.
What is contract cosmetics manufacturing?
Contract cosmetics manufacturing is producing a brand's products in a certified third-party facility rather than its own. Formulation, raw material sourcing, production, filling, packaging and regulatory filings sit with the manufacturer, leaving the brand owner free to focus on sales and marketing.
What is the minimum order quantity (MOQ)?
MOQ varies by product type, packaging format and formula complexity — higher for liquids and high-volume categories, lower for dermocosmetic serums. We share current category-level MOQ ranges when we respond to your quote request, within 24 hours.
How long until a product is shelf-ready?
With an existing formula the process typically runs 8–12 weeks. With formulation from scratch, stability testing and registration included, it can extend to 4–6 months. Stability testing is the single biggest driver of the timeline.
Can you produce using my own formula?
Yes. Our technical team reviews your existing formula for manufacturability and regulatory compliance, and adapts it where needed. Your formula is handled under a confidentiality agreement.
Do you handle the regulatory process as well?
Yes. Responsible technical person assignment, Ministry of Health notification, ÜTS registration, product safety report and SDS preparation, plus trademark and barcode registration are all included. You do not need a separate regulatory consultancy.
Do you source the packaging?
We identify packaging and carton options that fit your positioning, then handle sourcing and application. Label and carton graphic design is also within our scope.
Can I get a sample, and is it charged?
You can request samples from our existing formula library. For bespoke formulas developed from scratch, sampling is treated as part of the development process and terms are agreed at the quotation stage.
Do you manufacture for export?
Yes. We prepare formulation, labelling and documentation to the destination market's regulations, and provide the certificates of analysis and technical files export requires.
How is formula and brand confidentiality protected?
All discussions are conducted under a confidentiality agreement. Formulas developed for you are produced only for your brand and are not offered to other clients.
Where is your facility, and can I visit?
Our facility operates on 4,000 m² of enclosed area in the Ankara Anatolian Organised Industrial Zone. We arrange site visits by appointment — we recommend seeing your manufacturing partner in person.
Let's build your brand together.
We respond to quote requests within 24 hours.
Briefs and formulas you share are handled under a confidentiality agreement.