Product

How CRA-IQ Works

CRA-IQ was founded by experts in clinical operations and artificial intelligence with a mission to eliminate repetitive monitoring tasks and accelerate clinical discovery.

Data Extraction

Connects seamlessly to EDC, CTMS, and eTMF systems to gather structured data.

Intelligent Analysis

Detects deviations and incomplete actions using NLP and clinical ontologies.

Automated Drafting

Creates Monitoring Visit Reports (MVRs),summaries, automatically.
50-70% faster completion time

Human Oversight

CRA reviews, edits, and signs off to ensure explainable, compliant output.

Smart SDV

(focus on high-risk datapoints)

Multilingual support

(reduces translation delays)

Built-in Audit Trail

(21 CFR Part 11 compliant)

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.

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