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Medical Device Chatbot
powered by AI

Hey, there!

I’m Smarty, your Scilife Med Dev assistant. 

My data bank is stored with regulatory knowledge from the Medical Device industry and I’m here to answer any queries you have.

Here are a few example questions you can ask me:

  • What is the difference between 21 CFR 820 and ISO 13485?
  • How should I conduct a management review according to ISO 13485?
  • What do I need to do if I want to develop a class II medical device?

I'm in the beta version, but I’ll soon get better! I might not have all the answers up my digital sleeve, but my knowledge base develops each day.


Smarty is here to help you with your questions about Medical Device Regulations (ISO 13485, 21 CFR Part 820, ISO 14971, MDR and IVDR), as well as QMS software.

Now, are you ready to leap from theory to action?

Discover Scilife Smart QMS