CE certification helps manufacturers demonstrate that applicable products meet relevant European Union health, safety, and environmental requirements. The process generally involves identifying applicable legislation and standards, conducting risk assessments, completing required testing or conformity assessment, preparing technical documentation, and issuing the necessary Declaration of Conformity. CE marking may then be applied where required. It is relevant to products such as machinery, electrical equipment, personal protective equipment, and certain medical devices. Understanding CE certification can help manufacturers support regulatory compliance, prepare products for applicable European markets, improve product safety, maintain proper documentation, and build customer confidence.