FDA SaMD Class I/II • IEC 62304 • DICOM Computer Vision

AI Medical App Development & FDA SaMD Engineering

Turn deep learning models into clinical medical devices. We build audited, production-ready AI software for radiology imaging, ambient SOAP voice scribing, and predictive patient risk stratification.

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100% IEC 62304 Compliant
ISO 13485 Quality Management
510(k) Submission Dossier Ready
< 50ms Edge Model Inference

Clinical AI Inference Core

Audited SaMD Pipelines
FDA Validated
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DICOM Computer Vision Models X-Ray, CT, and MRI lesion segmentation with OHIF / Cornerstone Web Viewer.
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Ambient Clinical Voice Scribe Whisper Med + LLM clinical summarizer generating structured SOAP notes.
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Design History File (DHF) Traceability Full software traceability matrix from clinical requirements to unit/V&V tests.
Clinical Machine Learning Lifecycle

Medical AI & SaMD Engineering Capabilities

We bridge biomedical algorithms and rigorous medical device regulation, ensuring your AI product passes regulatory muster and clinician adoption.

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DICOM Imaging & PACS AI Integration

Deploy high-throughput DICOMweb inference servers interfacing with hospital PACS/VNA systems. Renders AI segmentations on zero-footprint web viewports.

DICOMweb / WADO-RS CornerstoneJS / OHIF PyTorch / TensorRT
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Ambient Clinical AI Scribing (SOAP)

Multi-speaker diarization and domain-specialized medical speech recognition converting natural doctor-patient dialogues into structured EHR encounter notes in real time.

SNOMED CT / ICD-10 HIPAA LLM Fine-Tuning FHIR DocumentReference
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IEC 62304 Software Lifecycle Controls

Software development plan (SDP), architectural design, risk management (ISO 14971), and software verification & validation (V&V) protocols for Class A, B, and C medical software.

IEC 62304 Class B/C ISO 14971 Risk Analysis Design Controls (DHF)
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On-Device CoreML & ONNX Edge Inference

Quantize and optimize deep learning models to run offline directly on patient iPhones and Android devices with sub-50ms inference and zero cloud latency.

Apple CoreML / Metal ONNX Runtime Mobile 8-bit INT Quantization
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Predictive Risk Stratification Models

Machine learning models predicting 30-day hospital readmissions, sepsis onset, glycemic excursions, and decompensation episodes from EHR and RPM telemetry.

Explainable AI (SHAP) Clinical Validation EHR CDS Trigger
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FDA 510(k) & De Novo Dossier Packaging

Compile comprehensive regulatory software dossiers, cybersecurity documentation, and clinical performance evaluation reports for FDA submission.

FDA 510(k) Pre-Sub Software Bill of Materials (SBOM) Cybersecurity Premarket
SaMD FAQs

Frequently Asked Questions About AI Medical Software

Under FDA and IMDRF guidelines, software intended to be used for diagnostic or therapeutic medical purposes (such as detecting anomalies in radiology scans or calculating drug dosage recommendations) is categorized as Software as a Medical Device (SaMD) and requires formal design controls (IEC 62304).

We implement automated DICOM de-identification pipelines removing all 18 HIPAA Safe Harbor identifiers and burned-in pixel text before ingestion, combined with federated learning architectures where raw PHI never leaves hospital networks.

Ready to Build Audited Medical AI Software?

Consult with our lead medical AI engineers and regulatory software architects to scope your model pipelines and FDA design history files.

💬 WhatsApp: +971 50 431 3932