Submitted by admin on Fri, 11/23/2012 - 19:29


During the 17th GHWP Meeting in Chinese Taipei, it has been agreed the adaption of "Guidelines for Regulatory Auditing of Quality Management Systems of Medical Device Manufacturers (Part 1-5)".

Please refer to the below attached with more information. 

Thank you.

(WG4 is referred to WG6 after the restructuring of work groups.)