Who We Are
•Kerevna is a boutique Contract Research Organization (CRO) delivering agile, high-quality clinical research solutions to biotech, pharma, and diagnostics companies.
•We specialize in providing hands-on support across the entire clinical development lifecycle, with strong focus on feasibility, site engagement, and operational excellence. Our boutique model ensures speed, flexibility, and personalized service.
•Kerevna collaborates with sponsors developing therapies across several areas including Infectious Disease and Wound Care.
A Boutique Approach to
Clinical Research
Comprehensive CRO solutions tailored to your unique project needs across all phases of development.
Clinical Trial Management
Protocol development, feasibility, site selection, and end-to-end trial management
Regulatory Affairs
Regulatory strategy, compliance support, and submission preparation
Data Management
EDC setup, CRF design, data validation, and submission-ready deliverables
Biostatistics
Study design, statistical analysis, and regulatory-compliant reporting
The Boutique
Advantage
Experience the perfect blend of Big-CRO expertise with personalized, agile service delivery
Avoid Big CRO Fatigue
Reduced bureaucracy and lower staff turnover compared to large CROs, ensuring consistent project management and faster decision-making.
Dedicated Expertise
Direct access to experienced specialists for deeper trial insights and faster decision-making without corporate layers.
Cost-Effective Solutions
Flexible, tailored engagement models aligned with your specific project scope and budget requirements.
Personalized, Client-First Approach
We work closely with sponsors as an extension of their team, providing direct access to experienced professionals and customized solutions—without layered bureaucracy.
Curated Global Site Relationships
Our strength lies in actively engaged, pre-vetted investigators and sites, enabling accurate feasibility, faster startup, and reliable study execution.
Proven Device & Outcomes Expertise
Extensive experience supporting medical device and outcomes-based studies, with strong understanding of regulatory, operational, and site-level requirements.
Agile Execution & Faster Decisions
With a boutique model and focused teams, we adapt quickly to evolving study needs, timelines, and protocol changes.
Quality-Driven, Inspection-Ready Processes
We maintain streamlined, compliant documentation aligned with ICH-GCP standards to support audits, inspections, and long-term study success.
Latest from Kerevna
Stay updated with the latest in clinical research and regulatory developments.
Ready to Elevate Your Clinical Trial?
Partner with Kerevna for agile, expert-driven clinical research support. Let's discuss how we can accelerate your study while maintaining the highest quality standards.