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Introduction to Critical Standards for Medical Device Development & Commerc...
Thu 13 April 2017, 14:00 – 17:00 SGT
The realization of a new medical device can be very costly and time consuming. Failure to meet the required level of quality, safety and reliability often lead to substantial set back to the organization, and sometimes its very survival. At this workshop, participants will find out about the essential international standards that are critical for the development and commercialization of medical devices. While some of these standards are regulatory requirements, this workshop will also highlight some important voluntary international standards that potential product owners should consider adopting during product development.
Speaker – Mr Liew Ee Bin, member of ISO/TC 210 WG1, JWG1 & WG6, Access-2-Healhcare
Who should attend?
Medical device R&D staff
Medical technology start-ups
Technology transfer office staff
How will I benefit?
Understand what are international standards
What standards are suitable for your work
Develop safe and reliable medical devices
WHat is included?
Certificate of attendance
Networking tea break
Date and Time
Singapore Manufacturing Federation
SMF House, Level 1, Classroom E1.4
2985 Jalan Bukit Merah
Singapore, Singapore 159457