Aiforia achieves CE-IVD mark for clinical PD-L1 AI model in lung cancer diagnosticsRead more
- Solutions by application
- Explore some of our use cases!
In EU and EEA countries Aiforia® Clinical is CE marked under the EU’s In Vitro Diagnostic Device Regulation 2017/746 for in vitro diagnostic use. In the USA, Japan, and other countries Aiforia® Clinical is for research use only and is not for use in diagnostic procedures.
*Aiforia's AI models and AI development platform, Aiforia Create, are currently sold with Research Use Status.
The browser-based Aiforia Clinical viewer removes the need to store or ship physical slides and there is no need for dedicated hardware to use the browser software.