Designed around the way
your specialty works.
Diagnostic interpretation and communication layered on Imaging’s study and archive.
Prioritize unread studies by urgency and subspecialty, assign readers and surface previous images/reports.
Provide structured templates, dictated text, organ-specific categories, lesion measurements and comparison with prior studies.
Manage preliminary/final reports, consultant verification, discrepancy review and addenda with recipient notifications.
Track urgent findings and incidental-finding follow-up through acknowledgement and action; include image-guided procedures with specimens and complications.
Diagnosis coverage and clinical records
Radiologist impression records findings and differential/definitive diagnoses with confidence and recommendation. Support fractures, masses, haemorrhage, embolic disease, infection and organ-specific disease; use BI-RADS/LI-RADS/TI-RADS/O-RADS only in their intended domains and versions.
Measurements that give the record meaning
| Measurement | Units / representation | Clinical context |
|---|---|---|
| Lesion dimensions | mm | Anatomical location, image reference, plane and prior match |
| Attenuation/signal descriptors | HU or qualitative | CT phase or MRI sequence |
| ADC | mm²/s | Acquisition and region-of-interest method |
| Organ/report category | named category | System, edition and applicable patient group |
| Stenosis | % | Vessel, segment and measurement method |
| Nuclear medicine uptake | SUV or method-specific value | Tracer, uptake time and normalization |
| Communication interval | minutes | Finding identified, message sent, acknowledged and escalated |
Equipment and integration plans
- Diagnostic viewers, PACS, speech recognition and approved AI orchestration → images, annotations, structured findings and signed reports.
- AI outputs remain attributed to model/version and input study, with human review; no automatic normal report or incidental-finding closure.
Connections require an approved interface and testing against the installed manufacturer, model and software. Listed equipment is a candidate integration target.
Explore equipment & roboticsReporting and meaningful outcomes
Report turnaround by urgency; critical finding acknowledgement; discrepancy review completion; recommendation follow-up with eligibility and time window.
Development scope and clinical validation
Initial scope
Report templates, worklists, sign-off, addenda and critical-result communication.
Advanced scope
Structured measurements, longitudinal lesion tracking and governed AI integrations.
Example acceptance scenarios
- An amended urgent finding must reopen the communication task even if the original report was acknowledged.
- Imported measurements require image/series association; a prior lesion cannot be matched solely by its size.
Research foundations
Research snapshot: 23 September 2026. References inform the proposed design; they do not certify FertPro or establish device compatibility. Diagnosis lists and measurement groups are not treatment protocols.