Your industry, our focus
Our international network of accredited electrical and electronics (E&E) laboratories and certifications bodies offer a comprehensive range of testing and certification services for active and non-active medical devices for gaining market access.
The CE mark is required for a variety of products in order to be legally placed on the market in the European Union.
The IECEE international Certification Body scheme (CB Scheme) test certificates and reports are accepted in over 50 countries.
From the 1st January 2021 the UKCA Mark replaces the CE mark for products placed onto the GB market.
Access the North American markets with the MET Mark NRTL product safety certification.
The Federal Communication Commission (FCC) is the US authority for the certification of telecommunication equipment.