Development of new medical devices for the market can be costly and time consuming. High standards of quality, safety and reliability often pose a challenge for organisations to meet its compliance. In order to help organisations cope with the challenge, Mr Liew Ee Bin, member of the ISO/TC 210 JWG1 was invited to share essential information regarding international standards that are critical for the development and commercialization of medical devices with 33 participants. He advised the participants on ways of coping with regulatory standards as well as highlighted the critical International Standards that are worth adopting for potential product owners as part of product development.
Participants had a very productive and meaningful afternoon as workshop speaker, Mr Liew Ee Bin, shared about adopting standards for Medical Device Development and Commercialisation