Category Archives: ce certification

Ultimate Guidance of Technical Files for Product CE Marking

The CE marking, which stands for “Conformite Europeenne” in French, attests to a product’s compliance with EU requirements for consumer safety, environmental protection, and health. To market their products in Europe, manufacturers both within and outside of the European Union … Continue reading

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What are the Most Common Reasons Why Customs Stops Products with CE Marking Issues?

Before a product is introduced to the EU market, it must comply with all mandatory requirements, as demonstrated by the CE marking conformity assessment procedure and subsequent application of the CE marking. Since the manufacturer often handles this process on … Continue reading

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Steps for Getting Your Medical Device CE Marked with EU MDR Requirements

The medical device needs to have a CE mark before it may be sold in the European Economic Area (EEA). The European General Medical Devices Directive’s “essential requirements” are met by the medical device according to the CE mark. Furthermore, … Continue reading

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Recognize the Types of Products that Require CE Marking

The main goal of the CE marking is to promote free trade of products inside the EU and lessen the impact of the actual boundaries between member states. Making the regulatory requirements for safety, health, and the environment consistent across the … Continue reading

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Understand the Six Steps towards Successful CE Mark Certification of the Product

A CE-marking is an important indication of the conformity of a product with the appropriate European product regulation. Though, a CE marking on a product only serves as an indication of its compliance. The CE marking of products allows free … Continue reading

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Understand the Process of Conformity to European (CE) Mark Certification

The CE marking signifies a manufacturer’s assertion that products comply with the EU’s new approach directives. These directives are not only implemented for products within the EU but also for products that are manufactured in or designed to be sold … Continue reading

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List of Procedures Required for CE Marking Structural Steel Documentation

CE Mark Documents for Structural Steel is designed and developed to guide steel structure manufacturing companies for CE certification as per DIN EN 1090 part 2 and ISO 3834 part 2 requirements. The CE Mark document set covers various types … Continue reading

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CE Mark Certification Requirement – CE Technical File

A CE technical file is a set of documents that describing a product and can demonstrate that the product is designed and in compliance with the requirements of a quality management system. All CE marking directives required a Technical File … Continue reading

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What to Document as Part of CE Mark Manual for Steel Structural Products

The documentation of CE Marking includes a manual to explain how to use the product safely. Mostly, the manual includes instructions for laypeople and service- maintenance instructions for specialized users. For consumer products, only a user manual is enough. Drafting … Continue reading

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CE Marking for Structural Steel

Since 1st July 2014, CE Marking for Structural Steel becomes mandatory for steel working in accordance with EN 1090-2 in European Union (EU) and European Economic Area (EEA). CE Marking is regulated by criminal law and the penalties for not … Continue reading

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