Core strengths

We help our clients develop life-changing treatments to improve patients’ health. We provide a tailored approach to clinical trial management focused on quality, value, and delivering results.

Core strengths

We help our clients develop life-changing treatments to improve patients’ health. We provide a tailored approach to clinical trial management focused on quality, value, and delivering results.


Unique risk sharing program: No Patients — No Payment

Rapid enrollment is supported by “No patients – No Payment” initiative, which means that the client reimburses Cromos Pharma only for enrolled patients and not for dormant, non-recruiting sites.

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Rapid patient recruitment and high retention rates

We believe in delivering efficient patient recruitment starting at the site level. This means selecting the right sites and working with them to maximize enrollment potential. We communicate closely with them to plan and manage local activities from translating protocols to designing effective pre-screening strategies to identify the right patients. This approach has resulted in an unparalleled track record in patient recruitment whereby our team met or shortened project timelines in 95% of conducted trials.

Reliable feasibility & venue/site strategy

Our experienced feasibility team will swiftly prepare a detailed capability / feasibility report. It will propose the optimal path forward, including country/venue strategy- and site-selection within the recommended venues. We offer free feasibility reports for Sponsors considering locating their trials in Central and Eastern Europe.

CPR: Capability → Plan → Rescue

More than half of all studies fail to meet enrollment timelines. If your study is behind schedule or encounters difficulties with recruitment/retention of subjects, Cromos Pharma can provide a comprehensive and collaborative rescue plan to ensure original investments yield a return and that the study is conducted efficiently. We offer the most rational and economical rescue plans to Sponsors to ensure the best value proposition at every stage of drug development.

Accelerated start-up

Our team of experts has years of experience successfully working with the FDA, EMA, and all relevant regulatory authorities across our regions. This in-depth local knowledge of submission guidelines and algorithms means that, depending upon the selected countries, your study will be up and running within 8-20 weeks.

Patients First

The welfare of our patients is our first priority. We are fully compliant with ICH-GCP and make sure that patients in our studies are well-informed, and have a direct line of communication to both the investigators and to our research team. Our multilingual Patient Portal provides relevant educational materials about clinical trials and patients’ rights.

Quality Management (Quality by Design – QBD)

Our Quality Management System is built upon Quality by Design principles that include integrated planning, quality agreements tailored to each project, real-time project risk-based analysis, data analytics-driven targeted monitoring, and customer-focused project optimization.

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