Gathering clinical evidence is the most expensive part of commercialising a medical app not submitting an application to the FDA.
ResApp will need to submit an application per disease starting off with pneumonia next quarter. Each algorithm will need to be approved by the FDA for each disease and will require seperate clinical evidence.
ePat are not diagnosing a life threatening disease, they are providing a tool to aid the assessment of pain and ultimately will need to submit less FDA submissions than RAP.
- Forums
- ASX - By Stock
- Ann: Update on ePAT for Infant Apps-MNQ.AX
Gathering clinical evidence is the most expensive part of...
-
- There are more pages in this discussion • 2 more messages in this thread...
You’re viewing a single post only. To view the entire thread just sign in or Join Now (FREE)
Featured News
Add MNQ (ASX) to my watchlist
Currently unlisted public company.
The Watchlist
BTH
BIGTINCAN HOLDINGS LIMITED
David Keane, Co-Founder & CEO
David Keane
Co-Founder & CEO
Previous Video
Next Video
SPONSORED BY The Market Online