CE Certification, commonly associated with CE marking, indicates that a product meets applicable European Union requirements for health, safety, and environmental protection. It is relevant to manufacturers and businesses placing certain products on the European market. The CE conformity process involves identifying applicable legislation and standards, assessing product risks, preparing technical documentation, and completing the required conformity assessment procedures. Depending on the product category, involvement of a notified body may be required. CE Certification can support market access, demonstrate regulatory conformity, and increase confidence among customers, distributors, and business partners. Maintaining appropriate technical records and monitoring regulatory requirements helps organizations continue meeting applicable CE marking obligations.