May 29 2019

Medical Device Software, Life Cycle Process, SaMD consideration and Cybersecurity

29 May 2019 09:00AM to 29 May 2019 05:00PM
NTU@One North, LT 301, level 3

Registration Date


10 May 2019 06:15PM to 28 May 2019 07:00PM

SMF Member Fee



GS1 Member Fee



Non-Member Fee



Event Details

Event Type


Seminars and Events

Industry Group


Medical Technology

Contact Person


Cherie Ong


 Software has enabled increasingly advanced functionality and interaction in medical devices. Software-driven user interfaces, stand-alone software applications, and mobile medical applications are becoming prevalent within the healthcare ecosystem.

The IEC 62304 standard for Medical Device Software – Software Life Cycle Process has been increasingly recognized by multiple regulatory bodies as a standard by which medical device manufactures can support regulatory compliance claims by implementing the process specified by IEC 62304.


At the end of the workshop, the target audience would understand the compliance importance of IEC 62304 with consideration for content of Software as Medical Device. UL 2900, a cybersecurity standard is included to have a completely effective software lifecycle from pre-market and post-market perspective.

Administrative Details

Programme is tentative and is subject to change at the sole discretion of Singapore Manufacturing Federation. 

Should you require further information or assistance, kindly contact
Ms Cherie Ong at 6826 3039.

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