Medical Image Analysis

We design and build custom medical image analysis software that helps clinicians read studies faster, quantify disease more consistently, and keep evidence audit-ready for regulators and partners. From classical computer vision in medical image analysis to deep learning–based detection and segmentation, we focus on AI that fits real clinical workflows.

Request an Imaging Assessment
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Our Offerings

Imaging Strategy & SaMD Advisory
Data & DICOM Infrastructure
Multimodal & Report Intelligence
3D Visualization & Surgical Planning
Radiation Therapy Planning Tooling
Deployment & MLOps for Imaging
Validation & Reader Studies
Security & Privacy Controls

Imaging Strategy & SaMD Advisory

We translate clinical needs into an imaging roadmap: target use cases, model fit, build-vs-buy, and the regulatory path for Software as a Medical Device (SaMD). We draft intended use statements, risk classification, and a clinical evaluation plan, then align software lifecycle with IEC 62304, ISO 13485 quality processes, and Good Machine Learning Practice principles. You get a phased plan with milestones, budget ranges, and regulatory compliance tracking built into the workstream.

Data & DICOM Infrastructure

We stand up the data layer that imaging AI depends on: DICOM gateways, DICOMweb, PACS/VNA connectors, and a versioned image lake in your cloud. Pipelines handle de-identification, harmonization, and labeling; metadata is normalized for robust cohorting. An OHIF-based viewer and annotation tools power review and ground truth creation. Everything is logged for audit and reproducibility.

Multimodal & Report Intelligence

We link pixels to context. NLP converts radiology reports into structured labels, ties impressions back to series/instances, and mines historical priors. We join imaging with EHR signals via HL7/FHIR to drive triage, quality checks, and outcomes tracking. The result is richer features, stronger training supervision, and decision support that reflects the full patient picture.

3D Visualization & Surgical Planning

We deliver interactive 3D tools for segmentation, registration, and measurement that surgeons and interventional teams can rely on during planning. Workflows include mesh generation, centerline extraction, volumetrics, and implant sizing, with export to standard objects and intra-op viewers. We can add AR/VR review or point-of-care planning for specific services where it adds value.

Radiation Therapy Planning Tooling

We integrate with RT objects, automate contouring with AI, and provide dose visualization, accumulation, and plan comparison. Tooling supports contour quality checks, margin application, and protocol templates so physics and dosimetry teams move from manual steps to guided, repeatable flows. Deliverables can include dashboards for plan QA and, where outcomes data is available, longitudinal toxicity metrics.

Deployment & MLOps for Imaging

Models ship as monitored services. We package inference with gRPC/REST, add a DICOM inference gateway for PACS round-trip, and manage GPU scheduling on-prem or in cloud. CI/CD, canary releases, model registry, drift/latency monitoring, and secure rollback are standard. You get live visibility into adoption, performance by site/scanner, and data drift alerts before quality slips.

Validation & Reader Studies

We design and run multi-reader, multi-case studies with predefined endpoints. Power calculations, case selection, site balance, and adjudication are handled end-to-end. Analyses follow study designs and statistical methods commonly used in FDA submissions, with a protocol, SAP, and a clean evidence package you can hand to regulators, clinical partners, or internal review boards.

Security & Privacy Controls

We implement PHI safeguards across the stack: end-to-end encryption, private networking, RBAC with least privilege, DICOM TLS, key management, and immutable audit trails. De-identification follows Safe Harbor or Expert Determination. We map controls to HIPAA and HITRUST requirements and set up ongoing compliance monitoring so access, changes, and data flows remain transparent.

Industries We Serve

  • Retail & eCommerce
  • Healthcare & Life Sciences
  • Finance & Banking
  • Logistics & Supply Chain
  • Manufacturing
  • Government & Public Sector
  • Startups
  • SaaS
  • Telecommunications
  • Education

Benefits You Get

Practical gains teams can plan for after a phased rollout and validation.

Faster reads and shorter turnaround

AI triage, pre-segmentation, and structured findings reduce minutes per study and flag urgent cases early. Radiologists keep working in PACS/VNA with zero app-switching, so the net effect is higher throughput at peak hours and fewer after-hours callbacks.

Reproducible measurements, less variability

Automated segmentation, volumetrics, and lesion tracking apply the same rules case after case. You get consistent quantification, tighter confidence intervals in studies, and cleaner longitudinal comparisons for tumor boards and follow-up clinics.

Lower run costs per study at scale

GPU pooling, batched inference, and edge–cloud split processing reduce per-study compute costs. Standard DICOMweb and HL7/FHIR keep interface fees down and avoid vendor lock-in, so adding new sites or scanners does not spike TCO.

Adoption without workflow friction

Everything sits inside existing worklists and viewers. Single-click QA, reversible overlays, and clear provenance help radiologists trust outputs. Training and SOPs focus on the few critical decision points that change behavior, not a long feature tour.

Audit-ready compliance posture

Immutable logs, role-based access, de-identification pipelines, and documented validation create a clean trail for HIPAA/HITRUST-aligned reviews. Centralized compliance monitoring and controls mapping make ongoing audits predictable instead of fire drills.

Future-proof architecture

Modular services, a model registry, and CI/CD for models make upgrades routine. You can iterate models, add new anatomies, or pilot third-party SaMD without reworking your data layer or integrations.

Want concrete gains and risks quantified for your setting?

Why Choose WiserBrand

We combine clinical-grade software engineering, SaMD know-how, and enterprise MLOps to take imaging AI from pilot to dependable production at health-system scale.

  • 1

    Regulated AI by design

    We don’t just “add models” — we design custom medical image analysis software around how radiologists, surgeons, and service line teams actually work. Every engagement starts from use cases, KPIs, and workflow maps, then brings in AI for medical image analysis only where it removes clicks, delays, or ambiguity.

  • 2

    Full-stack imaging & integrations

    Our teams work with DICOM/DICOMweb, PACS/VNA/RIS, and HL7/FHIR. We set up de-identification pipelines, labeling workflows, OHIF-based review tools, and cloud GPUs on AWS, Azure, or GCP that coexist with legacy systems. The result is repeatable ingestion, reliable routing, and vendor-neutral deployment options.

  • 3

    Proof-to-scale delivery

    We move imaging AI from scoped PoCs to controlled rollouts using reference architectures, a model registry, canary releases, and site-level monitoring. Success metrics stay clinical and operational — time-to-read, variability, sensitivity/AUC, throughput, and total cost per study — so leadership sees progress in terms that matter.

Our Experts Team Up With Major Players

Partnering with forward-thinking companies, we deliver digital solutions that empower businesses to reach new heights.

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Our Workflow

A phased path that reduces risk, exposes ROI early, and keeps clinical users in the loop.

01

Discovery & Use-Case Prioritization

We align clinical goals and business metrics with radiology leads and IT, then select one or two high-leverage use cases. KPIs, risks, and regulatory posture are defined up front so scope, timelines, and success criteria are unambiguous.

02

Data, DICOM & Security Foundation

We connect to PACS/VNA via DICOM/DICOMweb, establish a versioned image lake, and set up de-identification, labeling, and an OHIF viewer for review. Access is controlled with RBAC, encryption, and audited networking to keep PHI protected from day one.

03

Model Development & PoC

We build or adapt models for the chosen task — segmentation, detection, report NLP, or multimodal fusion — and evaluate across scanners and sites. Results cover accuracy, latency, and impact on reader time so leadership sees a clear go/no-go path.

04

Clinical Validation & Change Management

We run a multi-reader multi-case protocol with predefined endpoints and adjudication, while preparing SOPs, training, and release notes. Radiologists stay in the loop through guided reviews, keeping adoption high and feedback rapid.

05

Deployment, MLOps & Scale-Out

We ship monitored inference services with DICOM round-trip, start in canary or shadow mode, and expand site by site. A model registry, CI/CD, and drift/latency monitoring keep performance stable, with a steady cadence for new anatomies and locations.

Frequently Asked Questions

What do you need from us to kick off?

Read-only PACS/VNA access, a small starter cohort spanning scanners/protocols, a BAA, and points of contact for radiology, IT/PACS, and compliance. We can proceed in parallel on security review and network whitelisting.

Do we need FDA clearance for this use case—and can you support it?

We help clarify intended use, risk level, and evidence expectations, and we align requirements, testing, and validation activities with that path. When needed, we prepare technical and validation documentation your internal regulatory team or external consultants can use in their submissions.

How do you integrate with our existing systems?

We connect via DICOM/DICOMweb to PACS/VNA, and use HL7/FHIR to exchange orders, reports, and demographics. For viewing and annotation, we deploy an OHIF-based web viewer or integrate with your existing viewer. No workflow detours—radiologists stay in PACS with round-trip overlays and series routing.

How is performance validated before a broader rollout?

We run retrospective testing across sites and scanners, then a multi-reader, multi-case study with predefined endpoints. Power calculations, case adjudication, and subgroup analyses reduce surprises in production and give leadership confidence in real-world impact.

Where does it run and how is PHI protected?

Options include on-prem GPUs, your cloud in a private VPC, or a hybrid model. PHI is kept inside your network boundary; traffic is encrypted, access is RBAC-controlled, and every action is logged. For research or vendor collaboration, we apply Safe Harbor or Expert Determination de-identification and dataset versioning.