CE certification (Conformité Européenne) is a mandatory conformity mark for products sold in the European Economic Area (EEA). It signifies that a product meets essential EU health, safety, and environmental protection standards. Manufacturers ensure compliance, draft an EU Declaration of Conformity, and affix the CE mark to freely trade across 30 European countries website : https://iasiso-europe.com/french/certification-marquage-ce-en-france/

**ISO 13485 Training** provides professionals with the knowledge and skills to understand, implement, and maintain a Quality Management System (QMS) for medical devices. The course covers ISO 13485 requirements, regulatory compliance, risk management, and auditing practices to help organizations improve product quality, ensure patient safety, and meet international regulatory standards. website : https://iasiso-europe.com/french/formation-dauditeur-interne-iso-13485-en-france/