Responsible for product introduction and transfer from R&D sites, other Teva factories or external factories for collaborative products. Validates products to ensure commercial viability in accordance with regulatory requirements in...
Be accountable for medical evaluation/interpretation of aggregate safety data of assigned products and non-assigned products, as required, including, but not limited to, signal detection and evaluation, dose escalation evaluations, regulatory...
Be accountable for medical evaluation/interpretation of aggregate safety data of assigned products and non-assigned products, as required, including, but not limited to, signal detection and evaluation, dose escalation evaluations, regulatory...
Extracts reports from Tevaโs global pharmacovigilance database and from the European pharmacovigilance database (EudraVigilance), used for preparing safety analyses, with the purpose of monitoring the safety profile of Teva pharmaceutical...
Lead activities necessary for the determination of the safety profile and the characterization, monitoring, and mitigation of risks of assigned products during clinical development and/or post marketing including, as applicable,...
Responsible for product introduction and transfer from R&D sites, other Teva factories or external factories for collaborative products. Validates products to ensure commercial viability in accordance with regulatory requirements in...