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CE Marking is your ticket to EU market access. ECM has helped countless manufacturers understand and meet the requirements of relevant directives for CE Marking. Our advisory, testing, and certification services will guide you through every step of the CE Marking process.
The CE mark, or formerly EC mark, is a mandatory conformity marking for certain products sold within the European Economic Area (EEA) since 1985. The CE marking is also found on products sold outside the EEA that are manufactured in, or designed to be sold in, the EEA. This makes the CE marking recognizable worldwide even to people who are not part of the European Economic Area.
Both as testing lab and certification body – notified body ECM can execute the necessary activities required for declaration and CE marking, including testing and evaluating your technical files. For directives where a Notified Body is required to be involved, e.g. Medical Devices Directive – MDD, ECM can issue the certificates required.