SIS Certifications -  What is CE Mark Certification
                     What is CE Mark Certification? 
CE Mark Certification is a certification mark that indicates conformity with health, safety, and 
environmental protection standards for products sold within the European Economic Area (EEA). It is 
required for many products that are sold within the EEA, including medical devices, machinery, toys, 
construction products, and electronics. 
The CE mark is a symbol that is placed on a product or its packaging to indicate that the product 
complies with the essential requirements of the relevant European Directives. It is a self-certification 
process where the manufacturer or authorized representative of the product within the EEA declares 
that the product meets the essential requirements of the applicable directives and has been tested 
and assessed accordingly. 
The process of obtaining CE Mark Certification involves several steps, including: 
1.Identifying the applicable directives and standards for the product. 
2.Conducting an assessment of the product to ensure that it meets the essential requirements of the 
applicable directives. 
3.Preparing technical documentation to demonstrate compliance with the applicable directives. 
4.Testing the product and obtaining any required certification or approvals. 
5.Affixing the CE mark to the product or its packaging and issuing a Declaration of Conformity. 
CE Mark Certification is important because it demonstrates that a product is safe and meets the 
essential requirements of the applicable European Directives. It also allows manufacturers to sell their 
products within the EEA without additional testing or certification requirements.