Symyoo is a full-scope 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 clients’ unique needs.
Services provided by Symyoo are comprehensive and exhaustive for pharmaceutical, biotechnology and life-science, and medical device companies.
Our services are including but not limited to, clinical development consulting, clinical directing and medical writing, clinical operation and management, regulatory affairs, data management, biostatistics, pharmacovigilance/pharmacoepidemiology, medical monitoring and safety reporting.
In this industry, every second counts and the on-time delivery is critical. We commit to meet your expectations both on time and budget, while providing the top quality services across all stages of clinical development processes.
We will work tirelessly with you to keep your clinical studies moving forward as rapidly as possible.
Symyoo’s service is fully compliant with current regulations and guidelines (i.e., ICH-GCP, ethical requirements, the Helsinki Declaration) in addition to our standard operation procedures (SOPs).