SERVICES
Clinical AI product validation
& testing
Structured, multi-country testing of clinical AI tools by active licensed healthcare professionalsNiv: reader studies, model validation, benchmark review, LLM and multimodal evaluation.
Built for FDA and EU AI Act requirements.
Model & benchmark validation
Clinical accuracy and safety review against
real practice.
LLM & multimodal evaluation
Clinical safety rating of AI outputs, across markets and languages.
Reader studies
Multi-reader, blinded panels with senior adjudication.
WHAT THIS INVOLVES - Evidence your product is safe before a patient sees it.
YOUR BRIEF
"Gastric biopsy grading for an EU submission. Three independent reads per case, adjudicated."
↓ Medcase match
GI-subspecialised pathologists signing out 80+ GI biopsies a week · licensed in target EU markets · senior adjudicator on the panel.
Brief →
match
HOW IT WORKS
02
We match
We match
the panel
Sub-specialty, geography, licensure.
03
Reads &
Reads &
adjudication
Blinded, protocol-driven, HCP-led.
04
Submission-ready output
Submission-ready output
Documentation for FDA / EU AI Act.
01
Define