Get compliant with ease


With tutorial, guided prompts and real-life examples, it is now so much easier to understand the requirements and how to comply. What’s best is that we have kept all the technical jargons away!


Utilise our intuitive Q & A interface to customise your documents. Setting up your internal procedures is so much easier now and most importantly, they fulfill the requirements of the standards!


We have connected the inter-department processes based on best practices. Assign tasks and receive timely reminders? Tracking key metrics to better manage your compliance? We have it all covered!


Stendard refreshes whenever these standards gets updated. Currently in-built for ISO 13485 and US FDA requirements, we are also adding other standards soon. Now scale into new markets with ease!


Stendard Updates

The features are very intuitive and relevant for small businesses. Many startups will benefit from it!
— Mr Ong Jeong Shing, Investment Director, Venturecraft

Providing hints, guidances and examples while we fill up the forms are very useful! I don’t think I have seen that before!
— Dr Tan Swee Jin, Technical Director, Clearbridge mFluidics

Stendard is the solution for compliance. Will highly recommend it to our incubatees!
— Ms How Pei Sin, QA/RA Engineer, SysteMED Pte Ltd

Stendard provides the framework for medical device startups to meet ISO 13485:2016. Highly recommended!
— Mr Amrish Nair, CEO, Biorithm Pte Ltd

Stendard will help medical device companies to meet the latest ISO 13485 requirements!
— Mr Adrian Ang, CEO, AEvice Health Pte Ltd