Pharmacovigilance System Master File MasterClass

Topics

• Contents & Information that should contain
• Registration & maintenance of the PSMF
• Change control and Versions
• Format and layout
• Responsibilities of the MAH
• Archiving and Storage

Who should Attend

• Potential PV Auditors
• Pharmacovigilance Auditors
• Vendors of Pharma Companies
• PV personnel
• QPPVs
• Business Development
• Regulatory Affairs Technicians
• Regulatory Affairs Managers
• Continuous Improvement Staff