How does CE marking address the safety of autonomous systems?

Oct 31, 2019 ... The CE marking reflects the manufacturer's commitment to comply with European legislation and is mandatory for placing a product on the common ... What is the meaning of CE marking? When a product is CE marked, it means that the manufacturer has verified compliance with the essential health and safety ... We are regulatory professionals who guide on specific requirements that must be met and obtain the medical device CE Marking. The CE mark found on many electrical products is a European Economic Area mandatory conformity mark. It is a mark to identify products that are being sold ... 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. A mark required for many products that must be assessed, before being placed on the market, to meet EU safety, health and environmental protection ... The "CE" marking is a European logo indicating that the manufacturer has complied with certain compliance requirements to which the product is subject, to put ... A CE marking enables your medical device company to market and sell your product throughout the European Free Trade Area. Manufacturers can place a CE (Conformité Européenne) mark on a medical device once it has passed a conformity assessment. The conformity assessment usually ... 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 ...