EU Cosmetics Regulation 1223/2009 Compliance
Complete compliance service for EU Cosmetics Regulation β CPSR, CPNP notification, Responsible Person designation, and ISO 22716 GMP from an experienced EU regulatory team.
Care Europe provides end-to-end EU Cosmetics Regulation 1223/2009 compliance: Product Information File (PIF) preparation, coordination with qualified safety assessors, CPNP notification, and EU Responsible Person services.
Every cosmetic product placed on the EU market must comply with EU Regulation 1223/2009 β one of the most stringent cosmetic regulatory frameworks in the world. This regulation requires a comprehensive Product Information File, a safety assessment by a qualified cosmetic product safety assessor, and notification through the CPNP portal before market placement. Care Europe manages this entire process for North American and international cosmetic brands seeking EU market access.
Product Information File (PIF) Preparation
The Product Information File is the cornerstone of EU cosmetic compliance. It must contain the product description, cosmetic product safety report, method of manufacture, safety and efficacy substantiation, and evidence of the claimed effect. Care Europe prepares complete PIFs that meet all requirements of Annex I to EU Regulation 1223/2009. We work with your existing technical documentation and coordinate with qualified cosmetic product safety assessors (CPSAs) to complete the safety assessment portion of the PIF.
CPNP Notification & EU Responsible Person
Before a cosmetic product is placed on the EU market, it must be notified through the Cosmetic Products Notification Portal (CPNP). The notification must be submitted by the EU Responsible Person β a legal entity established within the EU. Care Europe manages CPNP submissions and can act as your EU Responsible Person, providing the legal foundation required for EU market access. We ensure all mandatory notification data is complete and accurate, including product category, frame formulation, and nanomaterial declarations where applicable.
Prohibited & Restricted Substances Review
EU Cosmetics Regulation includes Annex II (prohibited substances), Annex III (restricted substances), Annex IV (permitted colorants), Annex V (permitted preservatives), and Annex VI (permitted UV filters). Care Europe conducts a comprehensive ingredient review against all EU annexes to identify prohibited or restricted substances in your formulations. Where restrictions apply, we advise on maximum permitted concentrations, labeling requirements, and alternative ingredients where substitution is needed.
Services & Methods Included
- β Product Information File (PIF) preparation
- β Ingredient compliance review (Annexes IIβVI)
- β CPNP notification submission
- β EU Responsible Person designation
- β Safety assessor coordination
- β Nanomaterial declaration assessment
- β Labeling compliance review
- β Claims substantiation review
- β GMP compliance assessment (ISO 22716)
- β Post-market surveillance framework
Regulatory Standards & Compliance
- EU Regulation 1223/2009
- ISO 22716 (GMP for Cosmetics)
- ISO 10993 (Biocompatibility)
- SCCS Guidelines
- EU Annex II/III/IV/V/VI
Industries We Serve
- Cosmetic Companies
- North American Exporters
- Skincare Brands
- Personal Care Manufacturers
- EU Market Entry Clients
- Private Label Brands
Request a Consultation
Tell us about your product and regulatory challenge. We'll respond within 24 hours with an honest assessment and clear next step.
Get a Free Assessment βFrequently Asked Questions
What is a Product Information File (PIF) and why is it required?
A Product Information File (PIF) is a mandatory technical dossier required by EU Cosmetics Regulation 1223/2009 for every cosmetic product placed on the EU market. It must be kept by the EU Responsible Person and made available to competent authorities on request. The PIF contains the product description, safety report, manufacturing information, and evidence of claimed effects. Without a complete PIF, your product cannot legally be sold in the EU.
What is the CPNP and how does the notification process work?
The Cosmetic Products Notification Portal (CPNP) is the EU's online notification system for cosmetic products. Before placing a cosmetic product on the EU market, the EU Responsible Person must submit a notification through CPNP containing product information, frame formulation, and other mandatory data. Care Europe manages CPNP submissions as part of our cosmetic compliance service, ensuring all required information is submitted correctly.
Do EU cosmetic regulations apply to products sold online to EU customers?
Yes. If you sell cosmetic products to EU consumers β including through e-commerce β EU Cosmetics Regulation 1223/2009 applies. You must have a designated EU Responsible Person, a complete PIF, and a valid CPNP notification. Distance selling does not exempt products from EU regulatory requirements. Care Europe helps online brands establish the necessary compliance infrastructure for EU e-commerce.
Why brands choose Care Europe for cosmetic compliance eu
Registered in France
EU regulatory partner with legal standing
Bilingual EN/FR
Reports in English and French
NAβEU Bridge
We understand both regulatory worlds
Related articles
Cosmetic Product Safety Report (CPSR): Full Requirements Guide
What is a CPSR? Who needs one? What must it contain? A complete guide to the Cosmetic Product Safety Report required under EU Cosmetics Regulation 1223/2009.
EU Cosmetics RegulationCPNP Cosmetic Notification: Step-by-Step Registration Guide
How to notify a cosmetic product through the EU CPNP portal. Step-by-step guide covering registration, required information, common errors, and timelines.
EU Cosmetics RegulationEU Cosmetics Regulation 1223/2009: Prohibited and Restricted Substances
EU Cosmetics Regulation (EC) No 1223/2009 Annex II lists 1,600+ prohibited substances. Annex III lists restricted ones. What manufacturers must know about both lists.
EU Cosmetics RegulationEU Responsible Person for Cosmetics: Full Legal Obligations
What is an EU Responsible Person for cosmetics? What are their legal obligations under Regulation 1223/2009? Who needs one and how to appoint them correctly.
Ready to start your EU cosmetic compliance eu?
Tell us about your product and target EU markets. We'll respond within 24 hours with a regulatory assessment and next steps.
Get a Regulatory Quote β