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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.

  • Assistance in the identification of the applicable directives and the most suitable procedure for the fulfillment of legislative obligations
  • Execution of all necessary tests (ECM Testing Service) for the verification of compliance with the requirements of the Directive
  • Execution of laboratory tests and inspections of the essential requirements of the products aimed at obtaining certificates and certificates of compliance required for the affixing of the CE marking (EC type examination)
  • Inspections and control of production at manufacturers, according to the option chosen by the customer
  • Rating for the approval of the management systems for quality