SEQ Services: Complying with European Cosmetics Regulation 1223/2009

  • Understanding the Regulatory Framework for Cosmetic Products

  • Responsibilities of the Responsible Person and Safety Assessor

  • Compliance Steps: From Dossier Management to Safety Assessments

  • SEQ Services for Cosmetic Product Compliance

  • Ensuring ISO22716 Cosmetics-Good Manufacturing Practices

Welcome to SEQ Services, your partner in complying with European Cosmetics Regulation 1223/2009. Our comprehensive services cover the entire regulatory framework for cosmetic products, ensuring compliance with the latest regulations.

  • Regulatory Framework: Explore SEQ’s expertise in navigating the European Cosmetics Regulation 1223/2009, replacing the Cosmetics Directive 76/768/EEC.

  • Responsibilities: Understand the heightened responsibilities on the Responsible Person and the safety assessor, reinforcing the link between the Product Information Pack (PIP), the Product Safety Report, and the Cosmetic Safety Assessment.

  • Compliance Steps: SEQ can act on behalf of clients for dossier management, submission notifications to Competent Authorities, declarations to Poison Centres, labeling requirements, safety assessments, and more.

  • ISO22716 Compliance: Ensure compliance with ISO22716 Cosmetics-Good Manufacturing Practices with SEQ’s dedicated services.

 

Contact Us: For expert assistance in preparing and auditing Product Information Files (PIFs), ensuring label compliance, substantiating claims, and navigating the REACH registration process, contact SEQ at enquiries@nerin.co.im. Discover how SEQ can streamline your cosmetic product compliance journey.

  • Product Information Pack (PIP) and Safety Assessment Link

  • Responsibilities of the Responsible Person

  • Compliance Steps Overview

  • SEQ’s Comprehensive Services: Dossier Management to Safety Assessments