Registration Date |
: | 07 Sep 2018 09:00AM to 27 Sep 2018 05:00PM |
SMF Member Fee |
: | $50.00 |
GS1 Member Fee |
: | $50.00 |
Non-Member Fee |
: | $50.00 |
Event Type |
: | Workshops |
Industry Group |
: | None |
Contact Person |
: | Kevin Tan |
The Singapore Standard SS 620 : 2016 – Good Distribution Practice for Medical Devices - Requirements were developed by Enterprise Singapore under the Singapore Standardisation Programme. This standard focuses on the medical device import and distribution-related activities and sets the requirements to ensure the quality and integrity of the medical devices throughout the distribution process. The Health Sciences Authority (HSA) has implemented the SS 620 : 2016 on 9 November 2017 and the SS 620 : 2016 will replace the HSA Good Distribution Practice for Medical Devices – Requirements, Revision 2.1 (HSA GDPMDS TS-01, R2.1) as the certification standard from 9 November 2020 onwards.
This workshop aims to help distributors and importers of Medical Devices to be familiarized with the SS 620 : 2016, the implementation plan and the transition period. The speakers will share on the differences between the SS 620 : 2016 and the HSA GDPMDS TS-01, R2.1.
Mr Kevin Tan