Modules In the Courses

• Clinical Research and Data Management
• Introduction to Pharmacovigilance
• Introduction to Adverse Events
• Regulatory Guidelines & Laws Governing Pharmacovigilance
• Adverse Event Reporting Method
• Individual Case Safety Report Processing
• Specific Event Scenarios
• Narrative Writing
• Reporting
• Case Assessment
• Pharmacovigilance Compliance
• Medical Coding
• Coding with MedDRA Guidelines