Processing adverse events reports from post marketing sources into Teva's global safety database:
The different sources / types of reports includes:Reports from the scientific literature, Teva partners (other pharmaceutical companies), Health Authorities, Non-interventional studies and other programs
The processing includes Adverse Events coding (in medical dictionary - MedDRA), drug coding in the Company Product Dictionary, seriousness and labeling assessment and submission to health authorities
Working in global environment: Interacting with other global PhV units and local PhV reps. around the world
Taking part in the development and maintenance of an efficient and robust Pharmacovigilance system.