IS360 Technologies is a deep-tech medical device company developing AI-powered EEG analysis infrastructure for India's healthcare system — from neonatal ICUs to geriatric memory clinics.
India has over 30 million people living with neurological disorders, yet fewer than 1,500 trained neurologists serve a population of 1.4 billion. The diagnostic gap is staggering — especially in neonatal care, where early EEG-based intervention determines lifetime outcomes.
IS360 Technologies was founded to close this gap. NeuroSync ERP™ brings clinical-grade SLDA-based EEG analysis, real MRI annotation, and tamper-evident reporting to every clinician with a browser — from AIIMS Delhi to district hospitals in Tamil Nadu.
Our platform is built to India's regulatory standards: CDSCO-classified, DPDP Act-compliant, and ICMR-aligned — so the data your institution generates is legally defensible and clinically rigorous.
"The goal was never to replace the neurologist. It was to give every clinician in India the tools that only the best neurologists in the world have access to."— Founder, IS360 Technologies
A complete clinical EEG workflow — from raw file upload to CDSCO-auditable report — in a single browser-based platform.
Supervised Linear Discriminant Analysis on EDF, CSV, MAT, and PDF EEG sources. Computes delta/theta/alpha/beta/gamma band powers, asymmetry index, PAZ score, and KSI classification automatically.
Actual MRI photographs (not diagrams) with canvas-overlaid electrode positions, lobe zones, and asymmetry annotations across 5 anatomical views: axial, sagittal, coronal, lateral, and superior.
Tier 1: Generic patient summary. Tier 2: Full SLDA analysis, STEM, NPSP cognitive metrics, and roadmap. Tier 3: Complete IRT intervention protocol with home programme. Each tier is RBAC-locked.
SHA-256 hash of every report payload — clinician, algorithm version, patient ID, result vector, and timestamp. Tamper detection built into every page footer and provenance strip.
Six distinct roles (Physician, Therapist, Lab, Caregiver, Student, Super Admin) with report tier access enforced at the platform level. No workarounds. No tier creep.
REST API for institutional integration — push EEG files programmatically, retrieve analysis results, and pull audit chain hashes into your hospital information system.
NeuroSync ERP™ was born from a collaboration between AI researchers, neonatologists, and regulatory specialists committed to solving a real clinical problem.
The v5 roadmap moves NeuroSync ERP™ from client-side audit to a fully immutable, regulatorily anchored blockchain infrastructure.
NeuroSync ERP™ is a product of deep collaboration between neurologists, AI engineers, regulatory specialists, and clinical informaticists.
Every partner plays a specific role in the clinical, academic, and infrastructure integrity of NeuroSync ERP™.
NeuroSync ERP™ was designed for the Indian regulatory environment from day one — not bolted on after.
NeuroSync ERP™ is classified as a Software as a Medical Device (SaMD) Class B under the Central Drugs Standard Control Organisation. SLDA outputs are clinical decision support — not autonomous diagnosis.
Full compliance with the Digital Personal Data Protection Act, 2023. Data minimisation, purpose limitation, right to erasure, and 30-day DPO response SLA are built into the platform architecture.
Aligned with ICMR Ethical Guidelines for Biomedical and Health Research involving Human Participants. Patient consent requirements and data anonymisation protocols are enforced at the upload stage.
Every generated report carries a SHA-256 tamper-evident hash linking the EEG file fingerprint, algorithm version, HMAC signature, clinician attribution, and timestamp. Phase 5 anchors to the CDSCO Merkle registry.
From a single NICU to a multi-site institutional deployment — NeuroSync ERP™ scales with your clinical practice.