Regulatory assessment
Review of formulas, ingredients, product classification and readiness for lawful placement of cosmetic products on the EU market.
EU cosmetics regulation
A clear regulatory path from formula to the European Union market
EUCRI connects product safety, CPSR, PIF, CPNP, the Responsible Person, GMP, labelling and claims in one consistent process tailored to your product.
Specialist servicesacross nine connected areas
HR and ENcontent and communication
Email firsta clear record of every decision
Zagrebmeetings by prior appointment
Specialist services
Regulatory support throughout the product life cycle
Each area can be a stand-alone project or part of a complete route to market.
CPSR and product safety
Preparation and review of the CPSR, toxicological assessment of ingredients, exposure, margin of safety and finished product safety.
PIF documentation
Preparation, review and maintenance of the Product Information File, including the CPSR, GMP information, evidence of effect and change control.
CPNP notification
Preparation, submission, verification and maintenance of CPNP notifications before cosmetic products are placed on the EU market.
EU Responsible Person
EU Responsible Person and regulatory representation services for cosmetic brands, manufacturers and importers, including ongoing compliance maintenance.
Labelling and claims
Regulatory review of labels, INCI lists, mandatory particulars and substantiation for cosmetic claims on packaging, websites and advertising.
GMP and ISO 22716
Gap assessments, documentation, SOPs, audits and practical support for cosmetic manufacturers implementing GMP and ISO 22716.
Specialist services
Regulatory support for formulation development, reformulation, fragrances, essential oils, testing, packaging, private labels and due diligence.
Regulatory monitoring
Monitoring of cosmetics legislation, SCCS opinions and ingredient restrictions, with impact assessment for formulas, labels and portfolios.
How we work
Documentation must describe the actual product.
The formula, safety assessment, PIF, manufacture, label, claims and CPNP record must remain aligned. Every project therefore starts by identifying the product, markets, regulatory roles and document versions.
You receive a clear record of gaps, priorities, responsibilities and next steps, with email communication and meetings where needed.
Regulatory knowledge
Latest expert guides
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 →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.