How can businesses protect their intellectual property when undergoing CE marking conformity assessment?

Jan 25, 2021 ... The way in which a manufacturer must CE mark its device depends on the type of device in question and the regulations (MDR or IVDR) that apply. A manufacturer in the EU can utilize applicable European harmonised standards and/or Directives to in order to affix CE marking. In the United States, ... The CE marking (an acronym for the French “Conformite Europeenne”) certifies that a product has met EU health, safety, and environmental requirements, which ... The CE marking shall be affixed before the product with digital elements is placed on the market. It may be followed by a pictogram or any other mark indicating ... 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 ... Journalists ... Marcy l'Étoile, France, April 7th, 2025 – bioMérieux, a world leader in the field of in vitro diagnostics, announces the CE marking of ... The CE Marking or CE Certification is mandatory for certain product groups in the European Economic Area (EEA), consisting of the 30 Member States of the ... Sep 1, 2023 ... CE Mark Directives for Wireless Devices. For wireless devices, it's crucial to adhere to specific directives that regulate their functionality ... 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.