Facing the increasingly fierce competition in the domestic medical device market, companies' demands for going overseas have increased significantly. Countries around the world have diversified access requirements for medical devices, which undoubtedly makes it more difficult for companies to quickly develop the international medical device market.
Kanglife has many years of experience in certification in the medical device industry and can help customers identify the target country’s requirements for quality management systems, product testing, product performance, technical documentation and agents, and formulate the best go-to-market strategy for quickly entering the target country.
(Click on the icon to learn more about each country’s medical device registration requirements and service content)