Since 2006, I have been working for innovative pharmaceutical companies, specialized in generic and originator products. I have built up extensive experiences in managing marketing authorizations, preparation of dossier parts and variation procedures. My RA expertise consists of providing strategic input in decision making process with regulatory, quality and production teams. At the same time compiling, writing CMC regulatory dossiers for worldwide use and handling health authority questions. Furthermore, I am also providing support for eCTD submissions worldwide. I am a service oriented minded person with hands-on mentality, working accurately and proactively.
What I mostly appreciate about working at Starodub is the dynamic, stimulating working environment with great team spirit and professionality of my colleagues. The cooperation with RA experts of different specialties provide an extensive valuable source of knowledge and experiences, which I believe is key to the success of this business.