Stendard collaborated with Singapore Manufacturing Federation (SMF) on two of their recent workshops for the medical device industry. The workshops covered the importance of standards adoption, with particular reference to the ISO 13485:2016 and the SS 620:2016 standards. Participants included Singaporean companies involved in the medical device industry (manufacturers, importers, exporters, distributors and wholesalers).
Today, we are happy to announce the extension of our Stendard First™ platform to include SS 620:2016 (GDPMDS)!
New companies going into the business of import, trade, storage, secondary assembly and/or distribution of medical devices, as well as those existing ones certified to the current HSA GDMPDS TS-01 will benefit from this important launch.
In less than 3 weeks’ time, we are launching for SS 620. If you are on HSA GDPMDS (TS-01), great news! It isn’t as difficult that you need to hire/engage someone to help, but it’s not that straightforward either. Leverage on our software Q&A to customise an updated set of documents to comply with the new requirements – all in less than half a day.
If you are just about to get into the business, it’s straightforward for you – Use Stendard First™ to help you comply with the requirements while you focus to startup your business.
As part of our pre-launch, we are keeping this service for free, based on a limited period.