How to ensure compliance of a cosmetic product in the European market?
Europe is one of the main drivers of growth in the cosmetics industry, both because of its high consumption of cosmetic products and its extensive capacity to export these same products. On a planet with a wide range of resources and in an era where the potential for innovation is ever-increasing, the demands associated with cosmetic products are growing in order to ensure that the end consumer can enjoy these products in the most effective and safe way.
A cosmetic product is defined as "any substance or mixture intended to be placed in contact with the external parts of the human body (epidermis, hair system, nails, lips, and external genital organs) or with the teeth and mucous membranes of the oral cavity, with a view, exclusively or mainly, to cleaning them, perfuming them, modifying their appearance, protecting them, keeping them in good condition, or correcting body odors."
The Responsible Person for these products must ensure that, prior to being sold, they undergo a specialized assessment to guarantee their safety. This assessment is based on the interpretation of two main regulations:
Regulation (EC) No. 1223/2009 of the European Parliament and of the Council of 30 November 2009 on cosmetic products;
Commission Regulation (EU) No. 655/2013 of 10 July 2013 laying down common criteria for the justification of claims used in relation to cosmetic products.
The interpretation of these regulations focuses primarily on the safety assessment of the ingredients used, correct labeling presentation, and other relevant parameters.
The Responsible Person must also ensure that no animal testing is conducted on the cosmetic product and that it is manufactured according to Good Manufacturing Practices (GMP).
Once this assessment is complete and the cosmetic product's compliance with current standards is guaranteed, a notification is submitted to the Cosmetic Products Notification Portal (CPNP), which enables the sale and distribution of the product.
Pharmilab, as a company specialized in providing these consultancy services, offers all the necessary support to ensure that product registration is handled effectively. Should you have any questions, we remain at your disposal.