What is the role of industry associations in providing guidance and support on CE marking?

We are regulatory professionals who guide on specific requirements that must be met and obtain the medical device CE Marking. All products imported or sold in the EU must have the CE Mark. Affixing the CE Mark to a product indicates that it has been tested and meets the required ... Sep 14, 2017 ... No. CE marking is compulsory for most products covered by the New Approach Directives. Products not covered under a New Approach Directive do ... The Conformité Européene (CE) Mark is defined as the European Union's (EU) mandatory conformity marking for regulating the goods sold within the European ... CE marking is a process that applies to a wide variety of products and one which manufacturers located in the EU or importers of goods into the EU must ... The CE mark is a mandatory European marking for machinery and equipment to indicate conformity with the essential health and safety requirements set out in ... This training course will provide answers to these questions, which arise in conjunction with the engineering, acquisition and commissioning of new and ... Products with the CE mark (“Communité Européenne”) show compliance with the harmonized European Norm (hEN) standards. CE marked products can be used throughout ... CE marking of bituminous mixtures is based on a 2+ assessment system, applying the EN 13108 family of standards. A CE marking enables your medical device company to market and sell your product throughout the European Free Trade Area.