Stendard is in Beta!

All of us in Stendard would like to thank our believers and those who have expressed interest to try out our software - Stendard is in Beta now! After many months of development work, Stendard Beta has been launched to allow all of you to try it out for yourself and to give us your precious feedback.

 
stendard_beta
 

We are looking for companies to join us in our beta program! If you are part of a medical device company in the following phase, Stendard Beta is for you:

  1. Involving in design and development of your medical device

  2. Seeking your first ISO 13485 certification and/or US FDA 21 CFR compliance

  3. Enthusiastically seeking certification in the next 3-5 months

Upon completion of the beta program and as a token of appreciation from you will stand to enjoy benefits of up to USD 6000, including additional subscription months and consultancy support from our partners, when your company adopts Stendard as the preferred compliance solution!

Find out more by speaking with us!

Stendard has been evaluated by international certification and industry groups to have met the requirements of ISO 13485:2016 and US FDA 21 CFR Part 820.


Stendard is a cloud based software that simplifies the process for medical device companies to fulfil international regulations, such as ISO 13485 and US FDA 21 CFR, before products are approved for commercialisation. Conventionally, such work is performed manually and is very time-consuming. Stendard is the first to help small businesses achieve compliance in a fast, convenient, scalable and affordable manner.

Interested to find out more? Visit our website or contact us directly!