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What documents do European buyers typically request for private label hair care (COA, SDS, stability, micro)?

European buyers for private label hair care typically request a Certificate of Analysis (COA), Safety Data Sheet (SDS), stability test reports, and microbiological test reports. These documents ensure EU regulatory compliance and product quality assurance.

EU buyer view Launch planning Updated: February 8, 2026
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Best for
US brand owners, Amazon/FBA sellers, distributors, and private label buyers
Core intent
Who submits, what data is needed, and how to plan timelines before production

Quick Answer (for busy buyers)

Here’s the buyer-first summary. If your brand name is on the label, you usually act as the responsible person and must ensure the listing is submitted and kept current.

  • European buyers for private label hair care products commonly require specific documents for regulatory compliance and quality assurance.
  • The Certificate of Analysis (COA) confirms each batch meets ingredient and performance specifications.
  • The Safety Data Sheet (SDS) is mandatory under EU CLP regulations for safe handling and transport.
  • Stability test reports, often covering 3-6 months under controlled conditions, prove product shelf life.
  • Microbiological test reports verify the absence of contaminants, essential for consumer safety.
  • In our factory workflow, we integrate testing early to avoid delays.
  • For example, stability testing typically takes 3 months, so we recommend starting during sampling.
  • Microbiological tests are quicker, around 2 weeks, but require final production samples.
  • Concrete details: MOQ for hair care starts at 3,000 units per SKU, influencing batch testing costs.
  • Sampling timeline is 4-6 weeks for formula and packaging approval.
  • Lead time for full production with documents is 8-12 weeks after approval.
  • We support all testing and documentation preparation, but final market approval depends on specific EU member state requirements.
Buyer outcome
A launch-ready compliance plan: inputs collected, roles assigned, and update cadence defined.
Most common blocker
Missing facility information + inconsistent ingredient/label snapshots across SKUs.
⚠️
This page is a practical buyer guide. For definitive requirements and updates, use FDA resources and qualified regulatory counsel.
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