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Technology Platforms & AI Solutions

Purpose-Built Solutions for Modern Life Sciences & Healthcare

Overview

Connected Solutions Built for Real Life Sciences and Healthcare Work

IQA’s solutions combine domain expertise, product thinking, and AI-driven innovation to support the workflows that matter most across clinical development, regulatory operations, data quality, oversight, coding, and real-world evidence. These are not generic technology tools. They are purpose-built platforms and AI copilots designed to work in regulated, data-intensive, and operationally critical environments.

From study build and clinical oversight to protocol intelligence, medical coding, data quality operations, and evidence generation, our solutions help organizations improve speed, visibility, traceability, and execution across the full life sciences and healthcare value chain.

Core Solutions

InductiveEDC
Next-Generation Electronic Data Capture

InductiveEDC

A metadata-driven EDC platform built to support faster study build, cleaner data capture, stronger oversight, and more efficient downstream execution across clinical research programs.

Metadata-driven auto build for faster study setup
Flexible eCRF design and configuration
Intelligent edit checks and robust data validation
Role-based workflows and secure access control
Real-time study oversight and operational visibility
Integration-ready architecture for connected ecosystems
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RBQM
Clinical Trial Oversight Intelligence

RBQM

A risk-based quality management solution that transforms clinical and operational data into actionable oversight, helping teams identify issues earlier and manage trial risk more proactively.

Centralized risk monitoring and review
Early signal detection and prioritization
Site and study performance visibility
Quality and compliance oversight
Cross-functional operational intelligence
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Prabandhan
Project Oversight & Meta-Analysis

Prabandhan

A unified project oversight and meta-analysis solution that brings together study operations, milestones, vendors, compliance, financial tracking, and cross-study visibility in one connected environment.

Study oversight and control tower visibility
Vendor, milestone, and dependency tracking
Financial and operational visibility
Cross-study coordination and governance
Execution monitoring and proactive alerts
Meta-analysis across studies
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TrialLattice
Clinical Trial Collaboration Platform

TrialLattice

A collaborative platform designed to streamline study start-up, strengthen site and stakeholder coordination, and connect workflows across study teams and partners.

Start-up workflow coordination
Site collaboration and activation support
Study readiness visibility
Structured stakeholder communication
Faster operational handoffs across teams
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ClinEvra
Metadata-Driven Workflow Orchestration

ClinEvra

A metadata-driven, end-to-end workflow orchestration solution that dynamically extracts study assets from protocols and transforms them into structured, downstream-ready outputs for database build, validation, trial domains, SDTM preparation, and regulated study execution.

Dynamic protocol asset extraction and interpretation
Automated database and data validation specifications
Test case and validation specification generation
Trial domain and SDTM specification generation
SDTM dataset creation with pre- and post-validation support
Accelerated eCRF design, build, and validation with minimal manual intervention
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CDQOps
Quality-by-Design Operations

CDQOps

A quality-by-design data operations solution that improves validation, review, and oversight across clinical data workflows through traceable issue management, consistency controls, and operational visibility.

Data quality monitoring and oversight
Issue detection, triage, and review workflows
Quality-by-design support across the data lifecycle
Cross-check and consistency controls
Operational visibility for data management teams
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Aushadhi
AI-Powered Medical Coding Platform

Aushadhi

An AI-assisted medical coding platform that streamlines coding workflows, improves consistency, and supports traceable human review across clinical trial and safety workflows.

AI-assisted coding and term suggestions
Coding review and verification workflows
Dictionary-aligned coding processes
Greater efficiency and coding consistency
Traceable human review and oversight
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Evidexia
Real-World Evidence Platform

Evidexia

A platform for real-world evidence generation that supports data integration, curation, analytics, and evidence development across real-world, observational, and post-market environments.

Real-world data integration
Evidence generation workflows
Registry and observational study support
Post-market and outcomes insights
RWE and HEOR enablement
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Ready to Transform Your Clinical Operations?

Schedule a personalized demo of any solution or discuss a custom platform configuration for your organization.