About Us

About CRA-IQ

Our Vision

Revolutionize clinical oversight with intelligent, ethical, and compliant AI automation.

Our Mission

Empower sponsors, CROs, and clinical teams with AI that improves data accuracy, reduces manual workload, and ensures compliance.

Myster Peasah

Founder and CEO of CRA-IQ Ltd
Our Leadership

Myster Peasah is the Founder and CEO of CRA-IQ Ltd, bringing over 18 years of experience in clinical operations within CRO and pharmaceutical environments.He has led global Phase I-III studies, Specialising in patient recruitment, site engagement, regulatory compliance, and cross-functional project leadership.Driven by a passion for innovation, Myster established CRA-IQ to harness Al-driven tools that enhance CRA performance, oversight, and data integrity in clinical research.His mission is to bridge human expertise with intelligent automation to make drug development faster, safer, and more efficient.

CRA-IQ is designed with regulatory integrity and ethical AI principles at its core.

Compliance & Ethics

CRA-IQ is built for trust and compliance with:
Human-in-the-loop oversight ensures CRAs remain accountable for all final documentation outputs.
Regular validation, version control, and security protocols ensure inspection readiness and auditability.

Why CRA-IQ

“Artificial intelligence built with clinical integrity.”

– Combines human insight with machine precision.
– Reduces operational burden while maintaining regulatory trust.
– Scales efficiently across multi-phase, multi-country studies.

FAQ

Frequently Asked Questions

CRA-IQ’s algorithms are trained on validated clinical datasets and reviewed by qualified CRAs.
Each AI-generated report maintains over 95% accuracy, with final human verification ensuring complete regulatory compliance.

No. CRA-IQ is designed as an AI co-pilot, not a replacement.
It automates repetitive monitoring tasks such as SDV summaries and MVR drafts, while CRAs retain full control and accountability over all final outputs.

Yes. CRA-IQ is built to align with:

  • FDA 21 CFR Part 11

  • ICH-GCP E6(R2/R3)

  • EU AI Act

  • GDPR & HIPAA

This ensures that all documentation is audit-ready and inspection-compliant.

Absolutely. CRA-IQ integrates with major platforms  as well as EDC, CTMS, and eTMF environments through secure API connections.

CRA-IQ supports multilingual documentation — including English, Spanish, French, German, and Japanese — helping global teams manage multi-country studies without translation delays.

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