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CE Marking (Conformité Européenne) is a mandatory certification for products sold within the European Economic Area (EEA). It is the manufacturer’s declaration that a product complies with applicable European Union (EU) safety, health, and environmental protection directives.
The CE mark indicates that a product meets all relevant EU directives and regulations, allowing it to be legally placed on the European market. CE marking is essential for manufacturers who wish to export products to European countries.
“CE” stands for Conformité Européenne, meaning “European Conformity.” It signifies that the product conforms to European Union standards and regulatory requirements.
Documentation requirements depend on the product category and applicable EU directives. Our experts at ISO CERTIFICATIONS provide complete CE consultancy, assisting in preparing technical files, risk assessments, conformity declarations, product testing documentation, and compliance reports.
We guide you through the entire CE marking process — from identifying applicable directives to testing, documentation, and declaration of conformity.
(Applicable directives vary based on product type and intended use.)
CE marking is required in all European Union (EU) member states and European Economic Area (EEA) countries, including:
Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Liechtenstein, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden.