On April 14th, the four-day 89th China International Medical Equipment Fair (CMEF) ended perfectly! With the theme of "Innovation and Technology, Smart Future", this CMEF attracted nearly 5,000 domestic and foreign exhibitors, showcasing thousands of cutting-edge products and technologies covering intelligent diagnosis, telemedicine, precision treatment, wearable devices and other fields.
As a service organization deeply engaged in medical device testing and certification, CETC conducted face-to-face exchanges with partners and enterprises in various industries at the exhibition, and provided detailed and professional analysis and answers to the questions that customers are concerned about, such as international and domestic new certificate registration, product standard upgrading and change, product renewal registration, clinical trial protocol design, animal experiment protocol design, and medical quality management system audit.
During the exhibition, Xu Lifu, deputy director of the active engineering department of our medical division, was invited to share the theme at the "Standardized Escort • Innovation Leading" Medical Device Clinical Trial and Industrial Development Deep Integration Summit, and reported on the requirements for active medical device registration and inspection, precautions for inspection, and analysis of common nonconformities in inspection, and the on-site response was enthusiastic.
Xu Lifu, Deputy Director of the Active Engineering Department of CVC Weikai Medical Division, China Electric Research Institute
About us
CETC has a "one-stop" service platform for the whole medical device industry chain, which integrates R&D, registration testing, animal experiments, clinical trials, registration consulting, production quality management system (GMP) construction counseling, and ISO 13485 certification. It has obtained the national CMA qualification certification and CNAS accreditation of multi-category medical device standards, and has the ability to provide testing services for performance, safety, EMC, biocompatibility, animal experiments, environment, materials, microorganisms, etc., which can provide enterprises with compliance services throughout the life cycle and help enterprises achieve a closed-loop of full-value quality from product research and development to production and listing.