Agenda
8:00 AM — 8:45 AM
8:45 AM — 9:00 AM
Opening Remarks9:00 AM — 10:30 AM
Session 1: Regulatory System Strengthening: A Global Perspective10:30 AM — 11:00 AM
11:00 AM — 12:30 PM
Session 2: Good Regulatory Practices in the North Africa Region and Beyond12:30 PM — 2:00 PM
2:00 PM — 3:30 PM
Session 3: Biotherapeutic Products and Biosimilars3:30 PM — 4:00 PM
4:00 PM — 5:30 PM
Session 4: Safety and Pharmacovigilance9:00 AM — 10:30 AM
Session 5: Medical Devices and in-vitro diagnostics10:30 AM — 11:00 AM
11:00 AM — 12:30 PM
Session 6: Sub-standards and Falsified Medicines12:30 PM — 2:00 PM
2:00 PM — 3:30 PM
Session 7: Innovative Approaches in Medicine Developments3:30 PM — 4:00 PM
4:00 PM — 5:30 PM
Session 8: Final Panel Discussion and Key TakeawaysHave an account?