Symyoo is a contract research organization (CRO) with proven expertise in managing phase I-IV clinical trials across a broad range of therapeutic areas.

Symyoo brings together highly qualified and committed professionals and strives to tailor each project to meet each client’s unique needs.

Services provided by Symyoo are comprehensive, including, but not limited to: clinical trial management, regulatory affairs, data management, biostatistics, pharmacovigilance/pharmacoepidemiology, medical monitoring, safety reporting, and medical writing to biotechnology, medical device, and pharmaceutical industries.

Symyoo’s service is fully compliant with current regulations and guidelines i.e., ICH-GCP, ethical requirements, the Helsinki Declaration, and sponsor or our standard operation procedures (SOPs).