Arna is a trained professional in market registration of pharmaceuticals and has a PhD in regulatory science, combining the need for knowledge with a keen interest in the regulatory environment and clinical trial requirements of pharmaceuticals.
Arna is goal oriented and organized, has initiative and functions well within a group.
Clinical trial protocols (PK, BE and efficacy)
Clinical study reports (PK, BE and efficacy)
The CTD dossier
Compilation and maintenance of Module 3/Quality
Research and Development