AI Built for Regulated Industries

Your industry has rules.
Your AI should know them.

VelorQ delivers domain-trained AI for Education, Healthcare, Pharma, and Life Sciences — where getting it wrong has real consequences.

NABH · NAAC · CDSCO · FDA · EMA
Full tasks, not half-answers
Six layers of data isolation
Live in 48 hours
Explore AI Agents → How It Works
🎓 AURA Education AI 🏗️ LearnForge AI 📝 ExamForge AI 🎓 TutorMind AI ✨ ContentForge AI 🗺️ Curriculum IQ 🎯 MentorIQ
📄
INPUT

Syllabus & Standards

Curriculum documents, NAAC framework, and learning objectives uploaded to VelorQ.

→
🤖
AGENT

ExamForge AI

AURA-powered agent reads the syllabus, applies Bloom's taxonomy, builds the exam paper.

→
🔧
TOOLS

Standards Checker

Validates questions against NAAC criteria, generates marking scheme and difficulty map.

→
✅
OUTPUT

Ready Exam Paper

Complete exam with answer key, marking scheme, and NAAC compliance report in minutes.

📋

Delivered in minutes: Exam paper, answer key, and NAAC compliance report — ready for faculty review.

How It Works

Three layers.
One complete result.

A brain that knows your industry, workers that complete full tasks, and specialist tools that do each job with precision.

01
🧠

The Brain — Domain AI Models

Each model is trained specifically for one industry. AURA for Education, SAGE for Healthcare, NOVA for Pharma. They understand the rules, not just the words.

AURA — Education
02
🤖

The Workers — AI Agents

Agents complete whole jobs — not just answer questions. They access your private data, call the right model, use specialist tools, and deliver finished work.

03
🔧

The Tools — Specialist Capabilities

Behind every agent are purpose-built tools — document reading, signal detection, compliance checking. Each tool does one job with precision.

9 Standalone
Choose Your Industry

Solutions built
specifically for your world.

🧠 Powered by AURA

Smarter education. Less admin.

Universities, coaching institutes, and corporate training teams face mounting pressure to deliver personalised learning at scale, maintain accreditation standards, and prove outcomes.

  • NAAC documentation takes months of manual effort
  • Creating exam papers consumes faculty weekends
  • Students struggle outside class with no 24/7 support
  • Learning outcomes are tracked poorly or not at all
Explore Education Solutions →
🏗️

LearnForge AI

Complete AI learning department

📝

ExamForge AI

Exam papers and question banks

🎓

TutorMind AI

24/7 personalised tutoring

✨

ContentForge AI

Documents to learning modules

🗺️

CurriculumIQ

Curriculum gap analysis

🎯

MentorIQ

At-risk student detection

6 agents for Education · View all →
🧠 Powered by SAGE

Cut paperwork. Protect patients.

Hospitals and health systems spend enormous time on accreditation preparation, clinical documentation, and compliance reporting — time that should be spent on patient care.

  • NABH and JCI preparation takes months
  • Clinicians lack real-time decision support
  • Patient inquiry management is slow and inconsistent
  • Staff training compliance is hard to track
Explore Healthcare Solutions →
🩺

ClinicalPath AI

Right protocol at the right moment

🏅

AccredPrep AI

Complete NABH/JCI pack in days

🤝

PatientIQ

Patient engagement end-to-end

💬

InquiryIQ

Automated inquiry resolution

🔬

LabIQ

QC laboratory optimisation

👩‍⚕️

TrainingIQ

Staff compliance tracking

7 agents for Healthcare · View all →
🧠 Powered by NOVA

Months compressed to weeks.

Pharmaceutical companies face constant pressure to accelerate drug approvals, monitor safety signals, and stay ahead of regulatory changes from CDSCO, FDA, and EMA — simultaneously.

  • Regulatory dossier compilation takes months
  • Adverse event monitoring requires round-the-clock attention
  • Multi-site clinical trial tracking is spreadsheet-dependent
  • GxP compliance documentation is manual and error-prone
Explore Pharma Solutions →
📋

RegIntel

Complete dossier in weeks

🛡️

SafeWatch

Continuous adverse event monitoring

🔬

ClinTrialOps AI

Live trial visibility

🔒

ComplianceGuard AI

No regulatory surprises

✅

BatchIQ

Automated batch release

📊

AuditIQ

Always inspection-ready

14 agents for Pharma · View all →
🧠 Powered by NOVA

Research, safety,
and regulatory excellence.

CROs, biotech, and research organisations need AI that understands clinical research frameworks, safety reporting obligations, and the complexity of global regulatory submissions.

  • Safety signal detection requires expertise hard to scale
  • Multi-authority submissions are complex to coordinate
  • Clinical trial disclosure management is fragmented
  • Validation and compliance documentation is paper-heavy
Explore Life Sciences Solutions →
📤

SubmitIQ

Regulatory submission management

⚡

SignalIQ

Safety signal identification

📊

ComplianceIQ

Continuous GxP monitoring

🗂️

RegistryIQ

Global registration tracking

🔬

ClinTrialOps AI

Multi-site trial management

🔎

AuditIQ

Inspection readiness

9 agents for Life Sciences · View all →

Expanding to more industries

FinanceRetailLogisticsMediaAgricultureManufacturingLegal
The Platform

Powered by domain-trained AI
built for your industry.

🧠

Domain-Trained Models

Three models trained exclusively on industry-specific data, regulations, and clinical frameworks.

🤖

Purpose-Built Agents

Each agent is designed for a specific workflow — completing the full task and delivering finished work ready for review.

🔧

Specialist Tools

Standalone tools for immediate deployment and agent-bound tools powering complex workflows.

🔒

Six-Layer Data Isolation

Your data never reaches another customer. Six independent architectural barriers. Immutable audit trail on every action.

Explore the full platform architecture →