ce certification helps manufacturers demonstrate that their products meet applicable European Union requirements for health, safety, and environmental protection. The process generally involves identifying the applicable EU legislation and harmonized standards, assessing product risks, completing the required conformity assessment, preparing technical documentation, issuing an EU Declaration of Conformity, and affixing the CE marking when applicable. CE marking is relevant to many product categories, including machinery, medical devices, electrical equipment, personal protective equipment, and other regulated products placed on the EU market.