Slovenija
The Cosmetics Act (Official Gazette RS, No. 110/03 – official consolidated text) and Act Amending Certain Act in the Field of Health (Official Gazette RS, No. 47/04) (ZdZPZ) provide for legal foundations for issuing implementing regulations that have transposed Cosmetics Directive 76/768/EEC with all amendments, and all technical directives amending and complementing it owing to any technical progress.
- Regulation (EC) No . 1223/2009 of the European Parliament and of the Council of 30 November 2009 on cosmetic products
- Regulation on the implementation of Regulation (EC) on cosmetic products (Official Gazette of RS , no. 61/13 )
- The law on the termination of the Act on cosmetic products ( ZPVZKozP ) (Official Gazette of RS , no. 91/13 )
- Rules on the method of sampling and laboratory testing of cosmetic products (Official Gazette of RS , no. 59/06 )
EU
- Regulation (EC) No . 1223/2009 of the European Parliament and of the Council of 30 November 2009 on cosmetic products and its Anexes and Amendments
Features:
REGULATION. 1223/2009
- Responsibility: defined Responsible Person (natural or legal person, the manufacturer or a consulting company)
- Dossier-PIF, more complex, more comprehensive and more professional: Data dossier on a cosmetic product + Report on the safety of the cosmetic product safety information + + Cosmetic product safety assessment)
- Notification: the EU Commission, central to all Member States of the EU (distributors must be individually identified)
- Labelling: The name of the responsible person (who keep the dossier-PIF)
- GMP: ISO 22716
- Nanomaterials: precisely defined, specifically notified 6 months before marketing