Clinova CRO is a Morocco-based Contract Research Organization supporting pharmaceutical, biotechnology, and medical device companies with clinical research, regulatory, quality, and market access solutions in Morocco, North Africa, and beyond. We provide flexible, locally driven support across the clinical development lifecycle, combining regional expertise with international quality standards. Our services include: • Clinical trial feasibility, site selection & study start-up • Clinical monitoring & project management • Patient recruitment & retention • Regulatory submissions & AMMPS support • Local Authorized Representative (LAR) services for medical devices & IVDs • Medical device registration & regulatory support • Real-World Evidence (RWE), registries & observational studies • Phase I, PK/PD & later-phase study support • eTMF, document management & inspection readiness • Quality management, audits & eQMS support • ISO implementation & certification support • Data management, vendor & supply-chain coordination • Training and clinical/regulatory consulting Our experienced team and network of investigators, KOLs, healthcare institutions, and regional partners help sponsors navigate local requirements, identify qualified sites, access diverse patient populations, and execute studies efficiently. Our experience spans multiple therapeutic areas, including oncology, rare diseases, metabolic disorders, neurology, immunology, hematology, and more. From Morocco to the world, Clinova CRO connects local expertise with global clinical development. Embracing Your Innovation. CRO+
1 open job2 employeesResearch Services 