Starting MOQ
Starting MOQ is subject to formula, packaging and market documentation; request a project-specific quotation.
Global Compliance for Cosmetics
Plan your formula, claims, packaging, and documentation for the market you intend to enter.
A practical compliance path begins before production. Connect your formula brief and launch claims to market-specific documentation, packaging information, and quality requirements early in the project.
Current operating facts
Operating facts for market-ready projects
Effective 2026-10-23 · Policy v2026.10.23.1
Quote response SLA
Within 1 business day after we receive a complete project inquiry.
Laboratory sample development
Target: 5–7 business days after the approved development brief.
Sample dispatch
Scheduled after sample approval; shipping transit is separate and confirmed with the destination.
Packaging confirmation
Project-specific after component sourcing, pack-compatibility review and artwork sign-off.
Bulk production
Target: 25–35 working days after the production-readiness gate is complete.
Production-readiness gate: Production timing starts only after formula approval, packaging confirmation, artwork sign-off, required market documentation, component availability and agreed payment conditions are complete.
Start with the launch market
Compliance planning is a product-development decision.
Market rules influence the finished product, but they also influence how you frame a concept, select ingredients, prepare documentation, and describe performance. Those conversations are most useful before artwork and final production decisions are locked.
European Union
Plan for product safety information, responsible-person requirements, notification, label content, and evidence appropriate to the market and claims.
United States
Align product category, ingredient and label considerations, safety substantiation, and applicable FDA expectations for the intended product and claims.
Global export markets
Build a documentation checklist around the destination country, distributor or importer requirements, local language, and product-category rules.
A market-readiness workflow
Make the documentation path visible before the launch timeline becomes urgent.
Requirements vary by product and market. The purpose of this workflow is to make the core questions visible early, so formula, artwork, production, and regulatory workstreams can be aligned rather than handled in isolation.
Read: Private-label skincare EU compliance guide- 01
Identify the destination market
Confirm the markets you intend to enter, the product category, and the local pathway that applies to your formula, label, and responsible parties.
- 02
Align formula and claims
Review product composition, claim direction, fragrance and allergen considerations, and the evidence or documentation that may be needed for the intended communication.
- 03
Prepare product documentation
Coordinate finished-product specifications, ingredient information, quality documents, stability work, packaging details, and other market-specific materials.
- 04
Verify launch readiness
Complete market-specific checks with your qualified regulatory partners before distribution. Requirements depend on product, claim, packaging, and jurisdiction.
Connect compliance to development
The strongest claims start with a defensible product brief.
The claim language on a finished pack should match the formula direction, available support, product category, and the rules of the destination market. Start those conversations while development choices are still flexible.
Next step