Our highly trained statisticians can assist you with both carrying out your clinical trial and analysing your study results. We provide support for study planning, report preparation, PK/PD analyses in biostatistics, medical writing, and coding, all according to international medical standards such as MedDRA, ICD, and WHO-DD. We can also help with setting up a comprehensive data management system in compliance with GCP guidelines, as well as with establishing interfaces to EDC/RDE systems.