CTI-CEM International is an EU notified body for the Machinery and Radio Equipment Directive. We provide services which help our clients to meet the legislative requirements before their products are put into the EU market. The services include but not limited to file review, on-site inspection, and EU type examination for products within our accredited scope,.
As a third party product certification body, we can also carry out product certification, risk assessment, factory production control audit, management system assessment, and system gap analysis.
With many years of experience helping clients meeting EU and international legislation requirements, we are confident and competent to provide effective and professional service to the various needs of our clients from different industries. We can provide you with the latest information on the mandatory requirements of all countries and regions of the world, including CE marking, FCC approval, and the CCC certification in China.
Our second-to-none professional service will be tailored to your specific needs. Please contact us now to find out how we can help you to achieve your business goals.
Pre-production inspection, manufacturing process inspection, production monitoring, pre-shipment inspection, supervision of loading, and other customized inspection services.
CTI-CEM provides audit services aimed to suit the specific needs of our clients. Our auditing team are competent to examine suppliers’ production capacity, manufacturing equipment, management and quality procedures, safety guidelines, and social responsibilities.
Professional training and comprehensive solutions for product certification, technical regulations, management improvement and consultancy.
We are experts in other directives such as the Low Voltage Directive 2014/35/EU, Toy Safety Directive 2009/48/EC, Outdoor Noise Directive 2000/14/EC all of which we have experience and knowledge as a notified body. We can also provide expert advice in other areas such as the Medical Devices Directive 93/42/EEC / Medical Device Regulation 2017/745.