Regularly visit health care professionals in various fields of care (primary care physicians and specialists); actively market and promote prescription drugs with doctors, hospitals and the general medical community (clinics, pharmacies, etc.); attend professional and medical conferences.
Preparing dossiers for new products for submission to the relevant regulatory and health authorities; preparing document for renewing marketing authorizations, preparing and submitting regulatory variations and handling all other requirements as dictated by the relevant regulatory and health authorities.
Supporting and guiding new manufacturing processes, improving existing manufacturing processes, data analysis and conclusions
Reporting side effects and adverse events to the relevant regulatory and health authorities. Review and analysis of relevant literature, processing and recording data.