With Leida regulatory AI data platform it is possible for you to fully focus on what you do best:
your medical innovation.
​
We will handle the ever changing and scattered regulatory jungle, keeping all your medical innovations constantly compliant and relevant.
​
Our AI backed regulatory data platform flags regulatory changes and keeps all your medical devices and software compliance under one platform.
We follow all the relevant regulation: EU MDR/IVDR, MDCG, IMDRF, Relevant Articles and Academic Documents.
​​​
It is time to disrupt the medical device innovation
and build a revolution that shatters traditional barriers and paves the way
for a future
where transformative healthtech breaktroughs are boundless and redefine
the limits of
human well-being
Keep up with dynamic regulation
Leida will keep your devices compliant consistently, automatically flagging changes in the EU regulation, reducing the risk of non-compliance. Our AI data platform solution continuously monitors regulatory changes, ensuring your business stays ahead of regulation and compliant at all times.
All devices in the same place
You will have all your Medical Devices in the same place in Leida AI data platform for a comprehensive view of compliance status, device certification process and clinical trials with budgeting and forecast tools.
