ERA Global Standards Certification provides quality advisory services for CE marking. Our experts provide detailed comprehensive study of the entire EU directives and hence enabling the manufacturers to comply with the regulation in no time. Our team ensures that the procedure and processes implemented in the production are in accordance to the directives. The discrepancies are addressed promptly and training is provided at all levels and processes to ensure the compliance with EU directives.
CE at a glance
Established in 1993 the CE marking is a key indicator of a product’s compliance with EU legislation and enables the export of product to European Economic Area (EEA). Abbreviation of French: Conformité Européenne meaning “European Conformity”, formerly EC mark is a mandatory conformity mark for products being sold in the EEA.
Why CE Certification?
- CE marking is a kind of trade passport for the European Marketplace.
- Only one set of laws and regulations to comply with in designing and manufacturing the product for the entire 27 Member States of the EU and EFTA countries Iceland, Norway, Switzerland and Liechtenstein.
- CE mark on the product is well known as quality product for consumers in Europe as the mark ensures the compliance of EU Directives.
- Products under EU directives are to be produced in Europe or can be imported with CE mark only.
Perform Testing (to be witnessed by a Notified Body) of the product as per concerned standard after identifying the right directive for the product.The testing laboratory prepares the Test report.The notified body will prepare Technical Construction File (TCF) and declaration for conformity.Apply CE Mark to the product with number corresponding to the notified body.
General Procedure for CE Certification
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