What are the potential legal consequences for placing non-compliant products on the market?

CE marking indicates that a product has been assessed by the manufacturer and deemed to meet EU safety, health and environmental protection requirements. CE marking is required for all in vitro diagnostic (IVD) devices sold in Europe. CE marking indicates that an IVD device complies with the European In-Vitro ... As of 1 January 2022 the 30 months countdown started to August 2024 when cyber security will formally be a mandatory requirement for CE marking of radio ... We are regulatory professionals who guide on specific requirements that must be met and obtain the medical device CE Marking. The CE marking is applied to the product by the manufacturer, not by any authority or third party. This also means that no certificate grants the right to use ... 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 Association are a leading provider of help, training, product assessment and testing for product compliance legislation. We can help you CE Mark ... Let us guide you through the principles of CE marking step by step. We explain many of the words used in the context of CE marking, and you can get answers to ... A mark required for many products that must be assessed, before being placed on the market, to meet EU safety, health and environmental protection ... CE marking certifies that a product like a medical device meets essential health, safety, and environmental requirements as per EU legislation.