2017 CIRS Seminars Review

In the first half year of 2017, CFDA already issued so many medical device related regulations, notifications, guideline, industrial standards and etc. that the medical devices supervision and management is becoming more standardize in China. In order to let our clients be aware of the new regulations, CIRS would hold the seminar with certern intervals for our clients.

The list of the past seminar

September 8, 2017----CIRS and Techcode successfully co-held the ‘Medical Device Software Registration and Technical Verification Strategy Seminar’ in Beijing, China.

July 21, 2017----CIRS, East Lake High-tech and Yuhang District Biomedical Association successfully co-held the ‘China& Europe and America Medical Device Registration and System Seminar’ in Yuhang, China.

June 29, 2017----CIRS, Tianjin Dongli Economic and Technological Development Management Committee and East Lake High-tech Co. successfully co-held the ‘Tianjin Medical Device Registration, Clinical Trials and production System Regulation Seminar’ in Tianjin, China.

June 28, 2017----CIRS successfully held the ‘Medical Device Registration Test and EMC Test Operation Practice Seminar’ in Hangzhou, China.

May 27, 2017----CIRS and Techcode successfully co-held the ‘Medical Device Industrialization and Compliance Seminar’ in Jiashan, China.

April 21, 2017----CIRS and Techcode successfully co-held the ‘Medical Device Registration, Clinical Trial and Quality Management System Seminar’ in Nanjing, China.

March 16, 2017-March 19, 2017----CIRS attended ‘Korea KIMES 2017 International Medical Device Exhibition’ in Korea.

March 14, 2017----CIRS and Hangzhou High-tech Industrial Park successfully co-held the ‘Medical Device Registration Seminar’ in Hangzhou, China.

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