Symyoo has worked perpetually to accelerate the development of safe and effective medical therapeutics across all major therapeutic areas for the biotechnology, pharmaceutical, and medical device industries.

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At Symyoo, you will find highly qualified and committed professionals, giving you practical insights, with proven expertise in managing phase I-IV clinical trials across all major therapeutic areas. Symyoo guides and accelerate the whole process of your clinical development to success with sponsor’s mindset. We commit to meet your expectations both on time and budget, while providing the top-quality services.

A Comprehensive Service Provider for All Phases of Clinical Research

Symyoo has provided comprehensive services, including but not limited to: early and late phase trials, post-market surveillance, observation studies and many others for biotechnology, medical device, pharmaceutical industries and research investigators.

  • The early phase development has taken up over 1/3 of Symyoo’s projects, thus we know how to find out the clinical relevance successfully, while securing the patients’ safety.
  • For pivotal, late phase trials, we know how to efficiently operate the multi-site, large-scale trials in a very complicated environment, compliant with ICH-GCP, regulations, and other global standards.
  • We have specialized team members, clinical advisors, biostatisticians, and CDISC capable data managers, having advanced knowledge and extensive experience for specific therapeutic areas like oncology.