EU ยท CLP & REACH

From Launch Panic to Market Clearance in 4 Days

How a Portuguese skincare brand cleared 8 SKUs for EU distribution with 72 hours on the clock.

Products Covered

8 SKUs

Turnaround Time

4 days

Outcome

Audit passed

Client Background

A boutique skincare brand based in Lisbon, selling natural cosmetic formulations into independent retailers across Portugal, Spain, and France. Their range had grown to 8 SKUs and they had just signed a distribution agreement with a multi-country European partner.

The Problem

Three days before their distributor's onboarding deadline, the brand's logistics partner flagged that the Safety Data Sheets supplied with their products were not CLP-compliant and would be rejected at the warehouse intake check.

Missing the deadline meant losing the contract โ€” and roughly 40% of their projected annual revenue.

What We Found

  • SDS authored in an older 13-section format, not the EU 16-section structure required by REACH Annex II.
  • Section 2 missing several required H-statements for fragrance allergens above 0.1%.
  • Section 3 disclosed substances inconsistently across the range โ€” some INCI names, some trade names.
  • Section 15 contained generic boilerplate with no reference to current EU regulation versions.
  • No SVHC candidate-list check on file for any of the 8 products.

Our Process

  1. 1

    Day 1 โ€” Intake & triage

    Received full quantitative formulas for all 8 products under NDA. Mapped each ingredient against ECHA's substance database and flagged the 3 SKUs with the highest compliance risk.

  2. 2

    Day 2 โ€” Classification & SVHC check

    Re-classified every mixture under CLP for physical, health, and environmental hazards. Ran each substance through Annex XIV, Annex XVII, and the latest SVHC candidate list. No SVHCs above threshold โ€” documented and dated.

  3. 3

    Day 3 โ€” SDS authoring

    Authored all 8 SDS in the EU 16-section format, in English and Portuguese. Aligned Section 2 hazard statements with Section 15 regulatory references and Section 3 composition.

  4. 4

    Day 4 โ€” Label review & handover

    Reviewed the printed CLP labels against the new SDS. Caught one undersized pictogram on a 50 ml jar. Delivered final document pack with version log to the brand and their distributor.

The Outcome

The distributor cleared all 8 products at warehouse intake on the first attempt. The brand kept the contract and has since used the same documentation pack for a follow-on audit by a French retailer โ€” passed without changes.

8 / 8

Products cleared

4

Days to delivery

2

Audits passed since

"We thought we were going to lose the contract. Chemply turned a panic into a documentation pack we still use today."

โ€” Founder, Lisbon skincare brand

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