หน้าที่ความรับผิดชอบ

• Provide scientific data and responses for the healthcare professionals and customers medical queries or requests.
• Review, evaluate and prepare product information for management team consideration
• Manage pharmacovigilance activities i.e. receive of safety case report, submission of the case report to the health authority and product owner, follow-up with the additional information for the case report, management and update of safety information database in compliance with the application regulations, standard operating procedures and product’s manufacturer requirements.
• Provide supportive information to the customer in case the adverse event occurs
• Perform post-marketing evaluation/product safety monitoring and liaise with the product manufacturer and related functions for risk management plan preparation and implementation.
• Responsible for other PV related activities i.e. local literature search, local PV related regulations, periodic-reconciliation of the AE & related safety information, document archiving as requested by the local health authority and product manufacturer.
• Cooperate with all related functions and concerned parties for PV and medical information management.