Where can manufacturers find the latest versions of EU directives and harmonized standards?

CE marking certifies that a product like a medical device meets essential health, safety, and environmental requirements as per EU legislation. The letters "CE" are the abbreviation of French phrase "Conformité Européene" which literally means "European Conformity". The term initially used was "EC Mark" ... CE marking is a mark that manufacturers use to indicate that a product meets relevant European Union (EU) legal conformity standards in terms of safety, health ... Mar 2, 2021 ... The FDA approval and CE-marking of Guardant360 CDx for tumor mutation profiling and as a companion diagnostic for Tagrisso (osimertinib) ... The Construction Products Regulation (CPR) is fully implemented from 1st July 2013 across the 27 European Member states. As a result, all construction products ... Feb 23, 2021 ... The CE-marking is a clear indicator of a product's compliance with EU legislation. It is thus not an indication the product was produced in the EEA or Turkey. The Conformité Européene (CE) Mark is defined as the European Union's (EU) mandatory conformity marking for regulating the goods sold within the European ... Mar 21, 2024 ... By using the Vitrolife CE marked medical devices, healthcare providers and patients can have greater confidence that the devices meet stringent ... A mark required for many products that must be assessed, before being placed on the market, to meet EU safety, health and environmental protection ... A CE marking enables your medical device company to market and sell your product throughout the European Free Trade Area.