The Pharmacovigilance QMS & Inspection Preparation is dedicated to emerging technologies and innovative methods in Pharmacovigilance and best practices and strategies for audits and inspection preparation.
The Pharmacovigilance QMS & Inspection Preparation covers topics such as:
- Regulatory Affairs
- Pharmacovigilance/Drug safety (QPPV)
- Medical Information
- Quality and Compliance
- Compliance
- Risk Management
- Management Staff Responsible for Running Inspections
- Pharmacovigilance Auditors
- Drug/Product Safety
- Employees (directly and indirectly) Involved in Inspections
- Information and Clinical Data Management
- Drug Development
- Clinical Safety
- Clinical Pharmacology
- Quality Assurance
- Research & Development
- Signal Detection
- Patient Safety
- Outcome Research
- Safety Surveillance
- Epidemiology
- Data Analysis
- Regulatory Affairs and Compliance
- Medical Affairs
- Information technology
The next Pharmacovigilance QMS & Inspection Preparation will be held on 20-21 May 2024.