SESEC IV launched webinar on “Registration Process and Standards used on the Imported Medical Device in China”

On 30th November, the Seconded European Standardization Expert in China (SESEC) organized webinar on “Registration Process and Standards used on the Imported Medical Device in China” in Beijing office. As one of the main domain SESEC concerning, SESEC is devoting to promote and extend European stakeholders’ understanding on China’ medicine and medical devices regulation and standards. Regarding the increasing inquiries, SESEC invited Mrs. Bo Fan, senior engineer of Tianjin Medical Devise Quality, to deliver a keynote presentation and introduced in detailed the current situation and the future development of China’s standards on registration of imported medical devices. Over 60 SESEC’s colleagues, partners and stakeholders of European standards organizations, institutes and companies joined online.

In order to improve EU-China’s standardization dialogue and cooperation, SESEC were planning to continually invite related authorities and experts to take party in the monthly webinars ongoing.