Healthcare and Beauty Supply Chain Strategies

CEE has been transformed into the Regulation (EC) No 1223/2009 which is applicable in each member state

This new EU Cosmetics Regulation forces the application of GMPs (Good Manufacturing Practices) according to the ISO Standard NF EN ISO 22716 which gives guidelines for the production, control, storage and shipment of cosmetic for each production site. Compliance with this regulation will help you to reduce your "non-quality" costs and returned goods, avoid recalls and optimise your supply chain.

In parallel to this, you must also make sure that your suppliers of raw materials, packaging components and point-of-sale articles respect the EU REACH Regulations.

Intertek provides quality and safety services to the health and beauty product industry which help our customers:

  • To increase sales at a worldwide level
  • To optimise their Production, and Supply Chain locally and globally

Throughout the life cycle of the product, Intertek can support you:

Raw Materials and primary container

  • Quality Control (QC) testing in the sourcing country
  • Inspection on site before shipment
  • Vendor qualification
  • GMP Audit for cosmetic ingredients (European Federation for Cosmetic Ingredients (EFfCI)) or packaging manufacturers
      

Production sites

Intertek offers GMP services to production sites to be ready for the new GMP regulations and the European law . This includes:

  • Quality management system
  • GMP Audits and gap analysis
  • Clean room qualification
  • Raw materials and product assessment
  • Consultancy and Training
      

Distribution

  • Preparation of the PIP (Product Information Pack)
  • Industry research study
  • To prove and support your claims
  • Recall system management
      

End-of-Life

  • Packaging and product life cycle analysis
Need help or have a question? +1 905 542 2900
 

Need help or have a question?

+1 905 542 2900
France
+33 2 32 09 36 36
APAC:
+852 2173 8888
UK/EIRE:
+44 (0)116 263 0330