To respond to regulatory changes and technological advancements, we will establish, maintain, and manage a global pharmacovigilance system, as well as drive transformation.
- Understand and comply with regulations regarding pharmacovigilance activities in Japan, the United States, Europe, and Asia.
- Establish and maintain a pharmacovigilance framework (committees, SOPs, contracts, education, etc.)
- Manage audits and inspections conducted by global authorities and partner companies.
- Plan, develop, and maintain IT systems related to safety information.
- Drive process transformation for pharmacovigilance activities on a global scale.