Certifications tailored to where you sell.
Tell us the market and the document list, tests and filings become part of your quote and your project timeline.
Short answer: every library formula comes with stability data, a COA and batch microbiology, made in an ISO 22716 (cosmetics GMP) facility. Extra tests and filings are quoted per market: a challenge test from USD 1,000 per formula, HRIPT from USD 3,000, an EU or UK file with the PIF, CPSR, notification and Responsible Person USD 800 per product and a Certificate of Free Sale USD 100.
Korea's export data and example US and EU labels
Rules by market: US, UK, Canada, Australia, Germany, Netherlands, Singapore, Ireland, New Zealand or all markets
Guides: label requirements by country, ingredient lists, PAO and claims, importing from Korea step by step, testing and our label proof check.
Certified and export-ready
- ISO 22716 (cosmetics GMP) certified factory
- FDA registered factory (US MoCRA facility registration)
- Government-recognized in-house R&D department
FDA MoCRA
Product listing and facility registration under the Modernization of Cosmetics Regulation Act, label review for INCI, net quantity and warnings, and help naming your US responsible person. Sunscreen is an OTC drug in the US and is quoted case by case.
CPNP and the PIF
Cosmetic Product Notification Portal filing, a product information file with the safety report (CPSR), stability and challenge test data. Without an EU entity you also need an EU responsible person; our team confirms the options per project.
SCPN
Submit Cosmetic Product Notification with a UK responsible person, mirroring the EU file so one test set covers both markets.
Cosmetic Notification Form
Your company or importer notifies Health Canada within 10 days of first sale. We provide the INCI list, product information, a Hotlist ingredient check and a check of your English and French label.
AICIS and TGA
Your importer registers with AICIS; we provide the INCI list and product information, and check your label. Primary sunscreens, and some secondary ones, must be in the ARTG before sale (TGA).
Cosmetic import notification
A label check for full ingredient labeling in Japanese, quasi-drug review for actives that need it, and the export documents your Japanese importer needs.
ASEAN cosmetic notification
The company placing the product on each market notifies its regulator before sale: Thailand FDA, Malaysia NPRA, Singapore HSA, Philippines FDA, Vietnam MOH or Indonesia BPOM. In Singapore the local manufacturer or importer notifies through PRISM. We provide the INCI list and product information, and check your label against the ASEAN Appendix II particulars.
GCC registration
Saudi SFDA and UAE Montaji registration files and a check of the Arabic label.
MFDS and KC
To sell in Korea, your brand registers itself as the Korean cosmetics responsible seller. We provide the documents and check your artwork against the MFDS labeling rules.
Ask
China NMPA filing, Latin America (ANVISA, COFEPRIS) and others are handled with specialist partners and quoted per project.
Our production facility
The plant we produce in, and the credentials behind every batch.
ISO 22716
International cosmetics good manufacturing practice, certified in 2022.
FDA registered factory
Cosmetic facility registration under MoCRA since 2023. Registered, not approved: the FDA does not approve cosmetics.
Dedicated R&D department
Recognized by the Korean government in 2022, with formulators who have more than 10 years in cosmetics development.
Venture company
The production company was designated a venture company in 2026.
Patent application
A manufacturing method for an eco-friendly shampoo, filed in 2024.
Small and medium enterprise
A confirmed Korean small and medium enterprise.
Clean, ethical and market-specific options
Formulated and documented to the standard your market and your customers expect.
Cruelty-free by default
Korea has banned animal testing of cosmetics since 2017. We test on volunteers and in the lab, never on animals.
Vegan formulas
Plant-derived and synthetic alternatives to animal ingredients, documented ingredient by ingredient.
Free-from lists
Paraben, sulfate, silicone, mineral oil, synthetic fragrance or alcohol free, with the certificate of analysis to prove it.
Clean standards
Ingredient screening against retailer clean-beauty lists, documented ingredient by ingredient.
In every shipment
- Certificate of analysis per batch
- Safety data sheet
- Full INCI list
- Certificate of origin (KORUS form for the US)
- Commercial invoice and packing list with HS codes
Documents per product
Available per product once the mutual NDA is signed. Your EU or UK safety assessor gets what they need for the safety report.
- Full INCI lists, with trade names on the composite list
- Allergen list of 81 substances, the EU rule since July 2026
- IFRA certificate, 51st amendment, for fragranced products
- COA, MSDS (issued 2020 or later) and composition of every raw material
- COA, MSDS and specification of the finished product
- Challenge test report with its method: ISO 11930, European Pharmacopoeia, USP 51 or PCPC
- 12-week stability test at 40°C and room temperature
- Microbiology for S. aureus, E. coli, P. aeruginosa and C. albicans
- Compatibility test with the packaging (CT)
- Manufacturing process chart with ingredients
- Manufacturer declaration and statement of microbiological purity
- cGMP or ISO 22716 certificate
On request
- Stability and challenge test reports
- Heavy metal and microbiology results
- Certificate of free sale
- GMP certificate of the filling line (ISO 22716)
- Product information file, safety assessment
What we handle for a US launch
The file a US shipment needs, prepared by our team as part of your quote.
- FDA MoCRA product listings, filed by our team
- KORUS certificate of origin so tariffs are calculated correctly
- HS classification agreed with our customs broker before the first shipment
