as assigned. Responsible for day-to-day adverse events case management including case intake, tracking Responsible for reporting adverse experiences or events (AE) or product quality complaints (PQCs) associated
Establish contingency plans and identify trigger events and responsibility for initiating corrective action
Establish contingency plans and identify trigger events and responsibility for initiating corrective action
Detect, assess, understand, and prevent adverse events. Facilitate medical queries Product lead ensure
Detect, assess, understand, and prevent adverse events. Facilitate medical queries Product lead ensure
all received Product Quality Complaints, Adverse Events and Medical Enquiries to the relevant person in
all received Product Quality Complaints, Adverse Events and Medical Enquiries to the relevant person in