What are the key performance indicators (KPIs) that businesses can use to track their CE marking compliance?

Jul 25, 2022 ... The ubiquitous emblem of the CE mark effectively determines which goods in key product categories can be legally sold within the European Economic Area. 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 ... A CE marking enables your medical device company to market and sell your product throughout the European Free Trade Area. Jan 14, 2023 ... Any new IVD placed on the EU market from 26 May 2022 must be developed, manufactured and maintained in accordance with this regulation to be CE marked. A product with the CE mark must not be harmful to people's health or safety, or to the environment. When a manufacturer puts the CE mark on a product, they are ... 360 Compliance is here to offer expert guidance and support through every step of the certification process, ensuring a smooth market entry. Many products are covered by these directives and, to be placed on the European market, must bear the 'CE' mark - it's a legal requirement. CE marking is the ... CE-marking services from SGS – meet the compulsory product safety directives you need to trade in the EU with effective conformity assessment services. Apr 26, 2023 ... CE is an abbreviation of the French “Conformité Européenne”, which means “European Conformity”. Countries within the European Economic Area (EEA) ... Journalists ... Marcy l'Étoile, France, April 7th, 2025 – bioMérieux, a world leader in the field of in vitro diagnostics, announces the CE marking of ...