EU GVP Module 1 Quality System
EU GVP Module 2 System Master File
EU GVP Module 5 Risk Management System
EU GVP Module 6 Management and Reporting of Adverse Reactions to Medicinal Products
EU GVP Module 8 Post-Authorization Safety Studies
EU GVP Module 9 Signal Management
EU GVP Module 10 Additional Monitoring
EU GVP Module 15 Safety Communication
EU GVP Module 8 Addendum 1 Member States Requirements on Non-Interventional Post-Authorization Safety Studies
