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Your Agile Partner in Clinical Development

Pre-ClinicalPhase I–IVRWE/HEORPMSRBQM-DrivenQuality by DesignReal-Time Visibility

OUR QUALITY FOUNDATION

The Integrity Behind Every Insight

Every deliverable is backed by globally recognized standards and certifications - ensuring data integrity, regulatory compliance, and client trust.

ISO 9001
ISO 27001
ICH GCP
FDA 21 CFR Part 11
EU Annex 11
HIPAA
GDPR
CDISC
GAMP 5
GCDMP
ISO 9001
ISO 27001
ICH GCP
FDA 21 CFR Part 11
EU Annex 11
HIPAA
GDPR
CDISC
GAMP 5
GCDMP
THE IQA ADVANTAGE

Why Sponsors and CROs Trust IQA

Full-service CRO expertise and AI-powered solutions, aligned under one accountable partner

Accelerated DeliveryAccelerated Delivery
Quality by DefaultQuality by Default
Full TraceabilityFull Traceability
Regulatory ConfidenceRegulatory Confidence
Partnership

Flexible Engagement Models

Choose the partnership model that best fits your organizational needs and maturity.

Full Service CRO

Complete outsourcing of your clinical trial from startup to closeout. We take full responsibility for delivery.

  • End-to-end management
  • Fixed price or unit based
  • Outcome focused
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FSP & Embedded Teams

Dedicated resources that integrate seamlessly into your existing teams and systems.

  • Resource flexibility
  • Process control
  • Scalable capacity
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GCC Enablement (BOT)

We build, operate and transfer a dedicated capability center for you in India.

  • Cost arbitrage
  • Talent ownership
  • Strategic control
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Proven Delivery at Scale

A proven delivery track record across all phases of clinical trials, BA/BE studies, medical devices, and preclinical programs backed by expert teams, quality-led execution, and AI-powered solutions

300+
Clinical Trials
Phase I - IV
700+
BA / BE Studies
Bioavailability & Bioequivalence
25+
Medical Device Studies
SaMD & Implantables
10+
Preclinical Programs
Preclinical Sciences
Therapeutic Experience

Delivery experience across a broad range of therapeutic areas, supporting clinical development, evidence generation, medical devices, and post-market programs.

OncologyOphthalmologyDermatologyGastroenterologyNeurologyCardiovascularHaematologyUrologyRare Diseases
Regulatory Experience

Support aligned to global regulatory expectations across clinical, device, data, and evidence-driven programs.

Food and Drug Administration logoPMDA logoMHRA logoEuropean Medicines Agency LogoCentral Drugs Standard Control Organization logoHealth Sciences Authority authorityTherapeutic Goods Administration logoMedsafe logo
Product Experience

Experience across pharmaceuticals, biologics, medical devices, and technology-enabled healthcare solutions

NCEsGenericsBiosimilarsVaccinesMedical DevicesDigital Health Solutions
TRUSTED DELIVERY. FUTURE-READY SECURITY.

Build with Confidence. Move with Speed.

From expert CRO delivery to AI-powered solutions, IQA helps you move faster with secure, compliant, and future-ready execution-including quantum-safe security capabilities enabled through strategic partnership

Talk to Our Team

Enterprise-grade security. ISO 27001 audited. HIPAA & GDPR compliant.