Undesirable effects and cosmetovigilance after product launch
How to receive, assess, document and report undesirable and serious undesirable effects associated with cosmetic products in the EU.
Read the guide →Service area 08 · specialist support
Additional specialist regulatory services
Complex projects often extend beyond a single document. Specialist support connects formulation, suppliers, laboratories, packaging and commercial timelines in a workable regulatory plan.
Scope of support
What we can deliver for your project
Regulatory support for formulation development, reformulation, fragrances, essential oils, testing, packaging, private labels and due diligence.
- 80Regulatory alignment of formulations during development
- 81Replacement of prohibited or restricted ingredients
- 82Reformulation following regulatory change
- 83Advice on product preservation
- 84Regulatory assessment of essential oils and botanical extracts
- 85Review of fragrance composition documentation
- 86Coordination of stability and compatibility testing
- 87Coordination of preservative efficacy and microbiological testing
- 88Coordination of SPF, UVA and water-resistance testing
- 89Coordination of dermatological and instrumental testing
- 90Regulatory review of packaging
- 91Preparation of products for private labels
- 92Regulatory support for importers
- 93Regulatory due diligence before acquiring a brand or portfolio
- 94Expert opinions and regulatory assessments
- 95Workshops for formulators, manufacturers and marketing teams
Project outcomes
From a question to an actionable regulatory solution
The exact scope is confirmed after reviewing the product, target markets and available documentation.
01
Targeted expertise for the issue at hand
02
Coordination of laboratories and evidence
03
Support for development and reformulation
04
Reduced regulatory risk before investment
Frequently asked questions
Before the project starts
Do you perform laboratory testing?+
EUCRI coordinates the selection of testing and expert interpretation of results; testing itself is entrusted to suitable laboratories.
Do you support private-label projects?+
Yes. The scope is adapted to the allocation of responsibilities between the brand, manufacturer and Responsible Person.
Can you perform regulatory due diligence?+
Yes, for an individual product, a portfolio or a project before a commercial decision.
New fragrance allergen labelling requirements: 2026 and 2028 deadlines
What Regulation (EU) 2023/1545 changes for fragrance allergen labelling, which thresholds apply and how to prepare formulas and labels for 2026 and 2028.
Read the guide →Reformulating a cosmetic product after regulatory change
How to plan reformulation after an ingredient restriction and align testing, CPSR, PIF, labelling, CPNP and packaging stocks.
Read the guide →Next step
Do you have a product or portfolio for the EU market?
Send us the essential product details, target markets and available documentation. We will respond by email.