China International Medical Device Regulatory Forum (CIMDR II) Go back »

2011-03-10 | All chapters

China Center for Pharmaceutical International Exchange
Notice on holding the Second China International Medical Device Regulatory
Forum (CIMDR) and Workshop on Medical Device Pre-market Evaluation

In order to strengthen the publicity of China medical device administration regulations and policies, promote exchange and cooperations among international medical device
administration and evaluation authorities, standardize enterprises’ operation, boost communications between enterprises and governments and enterprises themselves, push forward application of new technical standards and technological achievements,
further improve safety and efficiency of medical devices, and, with SFDA’s approval, China Center for Pharmaceutical International Exchange will hold the second CIMDR from June 7, 2011 to June 10, 2011.

Moreover, in order to satisfy the need of many medical devices manufacturers in better understanding the international pre-market authorization regulations, such as application and approval procedures and technical review requirements, a workshop on medical device pre-market evaluation will be held on June 11 as a supplementary
session of the forum. Representatives from China and foreign medical device supervision departments, GHTF, medical device technical review institutions at home and abroad, standardization institutions and medical device enterprises will give speeches and
interact on the CIMDR.

We look forward to your participation!

For more information, please go to  CIMDR II Website  for the full notice in Chinese and English.

If you would like to know more detailed information about this event, please kindly contact the Business Managers of the HCE WG.