EU Cosmetics Regulation Services
Intertek provides you support through every step of the business process. From R&D, production, distribution, through to market support, Intertek enables clients to comply with ease to Regulation (EC) No 1223/2009.
Effective 11 July 2013, the European Union (EU) Cosmetics Directive 76/768/EEC will be replaced by the Cosmetic Products Regulation 1223/2009, which harmonizes and simplifies the cosmetics regulations across the EU member states. The goal is a higher level of consumer protection from hazardous substances and the lists of prohibited and restricted ingredients are provided in Annex II and III respectively.
Manufacturers must submit a product notification to the designated competent authority and prepare a product safety assessment and Product Information File (PIF). An understanding of the regulatory requirements is needed to successfully document safety, manufacturing information, and appropriate label information.
EU Cosmetics Directive Services
Intertek’s experts provide cosmetics companies with complete scientific and regulatory support for compliance with Regulation (EC) No 1223/2009 to keep their products on the European Union (EU) cosmetics market, including but not limited to:
- GMP (Good Manufacturing Practices) Certification
- Cosmetic Safety Assessments
- Cosmetics Ingredient Profiles
- Product Information Files (PIFs)
- Part A Cosmetics Product Safety Information
- Part B Cosmetic Product Safety Assessments
- Regulatory Compliance Support
- Regulatory advice
- Product notifications
- PIF assembly
- Clinical Studies for Claim
Substantiation
- Design, placement, and monitoring
- Product Labelling Review and Support
Request more information to see how Intertek can help your organization with EU Cosmetics Regulation Services.