Skip to main content

Health

Certified software for healthcare and pharmacy
MDR
IVDR
EU AI Act
RGPD Art. 9
HL7 FHIR

Our experience in Health

AI-powered diagnostic support systems, telemedicine platforms, clinical trial management, and pharmacovigilance tools. All our healthtech developments are designed to comply with MDR, IVDR, and the EU AI Act's high-risk classification.

Stages of the service

MDR/IVDR compliance for software as a medical device (SaMD)
High-risk AI according to EU AI Act (diagnosis and triage)
HL7 FHIR Interoperability
Protection of sensitive health data (GDPR Art. 9)
Results in the sector
95%
Sensitivity in AI triage models
0
Non-conformities in MDR audits
FHIR R4
Interoperability Standard

Do you have a project in healthtech & life sciences?

Tell us about your challenge and we'll propose the best architecture with guaranteed regulatory compliance.

Talk to a TWT architect