Poseidon CRO is a full-service clinical research organization committed to delivering high-quality, patient-centric studies across pharmaceuticals, biotechnology-derived products, stem cell therapies, medical devices, IVDs, and nutraceuticals.

We support companies of all sizes with agile, scalable clinical and regulatory solutions, integrating advanced digital tools, AI-driven insights, and local market expertise to accelerate development while ensuring full compliance and scientific integrity.

Our clinical operations are grounded in the latest industry guidelines and international GCP standards, covering the full study lifecycle—from feasibility and protocol design to regulatory submissions, site activation, interim monitoring, data management (eDC), pharmacovigilance, lab coordination, IMP oversight, data verification, and medical writing. We ensure a complete, end-to-end approach that enables successful trial delivery with quality, timelines, and cost-efficiency in focus.

Poseidon CRO’s Regulatory Affairs Department works in close synergy with clinical teams to manage submissions, amendments, and communications with Ethics Committees, Competent Authorities, and Ministries of Health across the regions we serve. Our mastery of evolving regulatory landscapes in Southeast Europe and North Africa positions us as a reliable partner in navigating complex compliance environments.

With over 15 years of regional experience and a strong emphasis on patient outcomes, digital health, and real-world evidence, Poseidon CRO leads with precision and care. Our multidisciplinary teams bring deep insight into Market Access, Pharmacoeconomics, and Health Outcomes Research, ensuring each project is not only operationally successful but also strategically impactful.

We make health our priority—by enabling innovation, assuring compliance, and delivering meaningful results.

Poseidon CRO

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