Did you know what is…
Cosmetic Regulation in the EU
The European Union Cosmetics Directive defines a cosmetic as “any substance or preparation intended to be placed in contact with the various external parts of the human body (epidermis, hair system, nails, lips and external genital organs) or with the teeth and the mucous membranes of the oral cavity with a view exclusively or mainly to cleaning them, perfuming them, changing their appearance and/or correcting body odours and/or protecting them or keeping them in good condition.
“The European Union requires that cosmetic products placed on the EU market be safe; that is, they “must not cause damage to human health when applied under normal or reasonably foreseeable conditions of use.” As in the U.S., manufacturers are responsible for ensuring that cosmetic products comply with the law before they are marketed. The manufacturer or importer of cosmetics is responsible for demonstrating that the product is safe for its intended use.
Regulations are enforced at the national level, and each country in the EU has an authoritative body that is responsible for upholding compliance.
As a consulting firm, specialized in technical and legal procedures for Cosmetics, the Biosanitary and Medical devices industry, we have many services to offer to your project
As a consulting firm, specialized in technical and legal procedures for the Biosanitary and Medical Devices industry, M Camps GTF offer you technical services por Span and e EU territory.
Assessment and preparation of the required documentation to obtain the Parapharmacy National Codes, for further presentation to the General Council of Official Colleges of Pharmacists
“No one better than her to talk about the regulatory issues concerning the industry”
“There are just a few Spanish cosmetic companies that have not contacted their cabinet at any time”
“Mercè Camps is a person with a great entrepreneurial spirit”