Seminar: Aligning your QMS for the EU market and how Stendard Flow™ can help!
Seminar: Aligning your QMS for the EU market and how Stendard Flow™ can help!

Workshop: The new EU Medical Device and in-vitro Diagnostics Regulation

Monday, 10 Jul 08:30AM - 11 Jul 2017 05:30PM (Asia/Singapore)


Stendard

Simplifying Compliance for Businesses

Stendard creates intelligent platforms to help companies adopt standards, build processes and accelerate their global growth. 

Starting with the MedTech industry, our first platform Stendard First™ has already supported 200+ companies in countries such as Korea, Germany, Australia, India and Singapore, through their QMS preparation to meet ISO 13485, SS 620 and other medical device standards. Our clients have also been successfully audited by Certification Bodies such as TUV Rheinland, SGS, BSI, TUV SUD and Socotec.