IRIS CRO is a full-service Clinical Research Organization established by experienced clinical research professionals.
We deliver high-quality, client-focused operational support across Latvia, Georgia, Poland, Lithuania, and Ukraine, ensuring speed, compliance, and predictable results for global sponsors.

Our multi-country footprint allows us to support studies with regional expertise, strong site networks, and fast regulatory timelines. We consistently meet deadlines, regulatory requirements, and enrollment milestones across all therapeutic areas and study phases.

Our leadership team unites experts with extensive industry backgrounds, committed to driving operational excellence and delivering successful clinical trials.

What we stand for:
✔ Full-service clinical operations across 5 countries
✔ ICH-GCP compliant processes and strong quality system
✔ Experienced CRAs, SSU & Regulatory specialists, and oversight monitors
✔ Fast start-up timelines in Eastern Europe
✔ Transparent communication and proactive issue resolution
✔ Flexible, sponsor-focused, solution-driven approach

IRIS CRO is dedicated to delivering reliable, agile, and high-quality clinical research — supporting sponsors from biotech, pharma, and medical device industries worldwide.

IRIS CRO

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IRIS CRO

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