CE Marking Certification allows you to legally export and sell your products in the European industry and state that it meets all relevant EU directives and rules. CE product marking will be a statement by the manufacturer that the item reaches the criteria that are suitable for health, security, and the environment described in relevant European product regulations and experiencing the appropriate conformity assessment operation.

CE marking needs vary from direction to direction, and even between directives. Our team marks experts who feel all these needs and can facilitate and tell you in every step of the process, from distinguishing the right direction, to improve the application of CE marking on your product. You can hire the CE marking guide to help you with the process of making a defined technical file with all the product details.

Products to be sold in the European Union (EU) that come under certain European Directives/Regulations must bear the CE mark. Here are some points mentioned to be considered.

CE requirements: – Manufacturer to assess whether the bodies that are notified are needed for CE marking.

Client application: – Manufacturer sends an application

Contract reviews: – 1. GenVitas Application Review 2. Request Additional Info 3. Prepare Offer

Client accepts Quote: – Manufacturers/service providers receive quotes

Module or system: – this step is different according to the categories and requirements of products expressed in the UE directive or regulations

Self-declaration: – manufacturer may be able to test its own product and/or factory production control

Marking CE: – Manufacturer applies the CE sign for their products