Axeon is ready to excel at any clinical trial operations project, whether it is a clinical trial we are leading as the only site, for clinical trials that we are participating in as one of many sites, or as a standalone service. We offer study design, project management, clinical trial site monitoring and management, data management, image analysis, statistics and statistical programming, medical writing, quality control, quality assurance, regulatory documentation, and data interpretation.

Axeon supports new drug development in every clinical stage with a strong focus on each stage of clinical trials and medical device studies.

• PIND/IND-Trials of New, Innovative, or Patented Drugs
• NDA-New and Patented Drugs
• ANDA-Generic Drugs/Off-Patent Drugs
• DMF-API/Active Pharmaceutical Intermediates
• BLA-Biological Products

Axeon offices are located in the USA, Australia and China and we conduct and manage clinical studies in accordance with International Conference on Harmonization-Good Clinical Practice (ICH-GCP) standards and all applicable regulatory requirements to pharmaceutical and scientific clients.