Candidate processing workflow
Deidentified data → U-Net/nnU-Net/SwinUNETR candidates → uncertainty/human review → research evaluation
JIVISION offers project development and technical assessment for Medical Imaging Research Algorithm Development. Scope: Research-only 2D/3D segmentation, lesion annotation and instrument tracking.
Research-only 2D/3D segmentation, lesion annotation and instrument tracking
Develop research software on deidentified data only, not diagnosis, treatment or clinical decision services; clinical translation requires separate approvals and validation.
These are candidate implementation paths. Establish a baseline on real samples, then select or combine methods for imaging, speed and deployment constraints. Model names do not imply measured project results.
Deidentified data → U-Net/nnU-Net/SwinUNETR candidates → uncertainty/human review → research evaluation
Provide raw sensor data, spectral bands or imaging modes, calibration files, acquisition conditions, control samples, reference truth and equipment-use constraints.
Research algorithms, experiment records, models and evaluation reports
Specify input formats, output fields, coordinates/units, error states, versions and invocation methods. Define review and failure handling. The statement of work determines the exact scope of source code, executables, model files or analysis reports.
Dice; HD95; case-level research sensitivity; calibration error; no device approval implied
Validate imaging quality, algorithm output and physical-value conversion separately. Use controls across media, devices, environments and acquisition batches, retaining raw data and parameters.
These are measures to agree and test, not achieved-performance claims. Freeze samples, reference truth, thresholds and hardware/software versions before acceptance; report subgroup results and failures, identifying under-sampled conditions as uncovered.
Agree targets, stations, inputs and responsibilities in a statement of work, separating required and excluded conditions.
Use representative samples to test critical risks, document feasibility/failures and scope the next-stage estimate.
Implement agreed functions and interfaces with configuration/change records; use offline replay before authorized device or site integration.
Retest against individual measures and hand over contracted artifacts with known limits; manage maintenance, expansion and changeovers as subsequent work packages.
Specialized imaging depends on sensors and calibration. Confirm equipment permissions, operator qualifications and intended use for radiography, thermography, remote sensing or medical research.
Candidate technologies are not license clearance. Check code, model weights, training data and dependency versions separately. Replace, license or exclude components unsuitable for the intended commercial delivery. Customer data is not used for public training by default.
Research-only 2D/3D segmentation, lesion annotation and instrument tracking. Deliverables: Research algorithms, experiment records, models and evaluation reports
Develop research software on deidentified data only, not diagnosis, treatment or clinical decision services; clinical translation requires separate approvals and validation.
Task-specific measures: Dice; HD95; case-level research sensitivity; calibration error; no device approval implied. Validate imaging quality, algorithm output and physical-value conversion separately. Use controls across media, devices, environments and acquisition batches, retaining raw data and parameters.
After reviewing samples for research-only 2d/3d segmentation, lesion annotation and instrument tracking, equipment conditions and interfaces, scope validation, development, deployment and acceptance separately. Data coverage, site changes and delivery rights affect the estimate; no fixed performance or schedule is promised before assessment.
Service ID: F17 · Medical Imaging Research Algorithm Development
Describe available samples, equipment and target measures. Agree confidentiality and permissions before transferring sensitive or personal data through an approved channel.
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