Poseidon CRO is a full-service clinical research organization delivering clinical studies in pharmaceutical development, biotechnology-derived products, Stem cell therapies, medical devices, and Nutraceuticals. We provide tailored solutions for pharma and business insights in related Market Access, Patient Outcomes studies, and Pharmacoeconomics. Within the clinical research department, all efforts are invested according to the most up-to-date industry guidances to deliver services of feasibility on the research project, protocols elaboration, submission to regulatory authorities, implementation, interim monitoring, validation and coordination of clinical biology services, pharmacovigilance detection, reporting and reconciliation of events, IMPs management, proper eDC solutions, data verification, and storage; site closures and medical writing, ensuring and end of end spectrum of solutions is provided to our customers. Poseidon CRO has pharmaceutical and regulatory expertise to provide scientific-technical support, high-level compliance with regulatory requirements. The regulatory assistance department is designed to be attached to the clinical research department regarding the preparation of clinical trial records and their submission to the authorities (IRBs/ECs, Department of Pharmacy, and MoH) and amendments made during a study. Mastering new trends in specific regulations in our markets make us leading the qualitative change of the industry and health-related insights southeast Europe and North African regions Our vision of excellence and the expertise acquired through the years makes us able to understand our client's needs and ensure a 360° coverage by the solutions we forge and implement.