Medical Affairs Director
Current- Research and development work to support the medical value of the products of EGIS; - Coordinating the workflow of the subordinate units with other parts of the organization;- Compilation and continuous revision of the clinical and non-clinical part of the registration documentation taking into consideration the actual regulations, regulatory requirements and medical knowledge;- Giving scientific support and/or medical background for decisions at different levels of the Company, elaborating proposals in relation to research and development activities;- Supervising, organizing and coordinating pharmacovigilance activities for medicinal products of EGIS, exercising the duties of the QPPV.