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Helping The Medical Device Industry To Seize The European Market
Oct 10, 2017

016 August 30 Afternoon, "the EU's latest regulatory trends, review the main points of new interpretation" symposium in Guangdong Bio-pharmaceutical industry base held. Under the new regulations and the increasingly severe EU market supervision background, EU law experts and the presence of enterprises to explore the medical device industry's development direction and coping strategies.

"Compared to the old and new two version ISO13485 can be found that the new approach to enterprise management requirements more stringent." "With the government's increasing supervision of medical devices industry, fully grasp the new rules in helping enterprises to achieve standardized management, but also better to help push enterprises to the international market."