When it comes to adverse events, medical information (MI) teams are very often the first point of contact and MI teams are required to channel that information to the safety pharmacovigilance team as soon as possible for effective and efficient triage. Once the case is registered in the safety system, information then needs to be communicated back to the MI teams.
How can the two systems, MI and Safety, be reconciled accurately? And can the whole process be optimized?
In this webinar you will learn about:
• The current adverse event reconciliation process
• Collecting adverse event data in an MI environment
• Exporting and managing adverse event data
• The benefits of automating the process