CE certification helps manufacturers demonstrate that their products meet applicable European Union requirements for health, safety, and environmental protection. It applies to various products, including machinery, electrical equipment, medical devices, toys, and personal protective equipment, depending on the relevant legislation. The process generally involves identifying applicable requirements, conducting risk assessments, performing necessary testing, preparing technical documentation, completing conformity assessment procedures, and issuing an EU Declaration of Conformity before applying the CE marking. CE certification can support regulatory compliance, access to European markets, product credibility, and customer confidence while helping manufacturers maintain consistent safety and quality practices.