Our people are organised into dedicated writing teams. Each dedicated team is made up of degree-trained scientists who provide medical writing, project management, and quality control. Each team has more than 20 years of cumulative experience writing clinical documentation for the global pharmaceutical industry. The Trilogy teams are fully conversant with ICH and GCP standards as well as US and European regulatory requirements, and have written hundreds of clinical study reports and dozens of CTD submissions.

Our people are provided with continuous professional development in new documentation requirements (e.g. the Paediatric Investigational Plan), updates to regulatory guidelines, and ongoing training from the European Medical Writers Association (EMWA) as well as the Trilogy in-house development programme. Our tightly-knit organisation allows us to share experience and share our common knowledge base.