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Pioneering Precision in Clinical Research

Innovative. Reliable. Compliant. Welcome to Kerevna, where science meets integrity.

Who we are?

Who We Are?

Kerevna is a globally recognized Contract Research Organization (CRO) offering a full spectrum of clinical development services. From startup biotechs to top pharmaceutical companies, we help you accelerate outcomes through scientific rigor and regulatory strategy.

Our Expertise

From early-phase trials to post-marketing surveillance, our services span the entire drug development lifecycle. We specialize in trial design, real-world evidence generation, remote monitoring, and global regulatory strategy.

Trial Management

Clinical Trials Management

Full lifecycle support from protocol design to site close-out with risk-based monitoring models.

Data Management

Clinical Data Management

High-quality data capture using EDC, CRF design, and real-time query resolution for submission-readiness.

Regulatory Support

Regulatory Support

Global regulatory filings, IND/CTA/ANDA submissions, and health authority interactions.

Why Choose Kerevna?

Our client-first mindset, global infrastructure, and therapeutic focus help sponsors bring innovative products to patients faster and more reliably.

Partner With Us

Looking for a reliable CRO partner? Kerevna provides strategic guidance and full-service execution from IND filing to NDA submission. We don't just manage trials—we accelerate innovation.