Registration
  • 8:00 - 08:30
Opening
  • 8:30 - 09:00
Plenary 1:
Smart Regulation: Global Benchmarking Tool, WHO Listed Authorities, GRP, Good Reliance Practices
  • 9:00 - 10:30
Coffee Break
  • 10:30 - 11:00
Plenary 2:
Pharmacovigilance
  • 11:00 - 12:30
Lunch Break
  • 12:30 - 13:30
Workshop 1:
GRP Implementation
Workshop 2:
GMP/GDP Inspections (including links with environmental aspects/AMR)
  • 13:30-15:00
Coffee Break
  • 15:00 - 15:30
Workshop 3:
QMS (NRAs and inspectorates)
Workshop 4:
SF Medical Products
  • 15:30 - 17:00
Pre-icdra Reception
  • 19:00 - 21:00

Please note that the agendas for Pre-icdra and icdra provide a draft outline of the event which will be updated regularly

Workshop 5:
Prequalification of medical products
Workshop 6:
API Quality
  • 9:00 - 10:30
Coffee Break
  • 10:30 - 11:00
Workshop 7:
Medical Devices & IVDs
Workshop 8:
Supply and Distribution
  • 11:00 - 12:30
Lunch Break
  • 12:30 - 13:30
Workshop 9:
Snake venoms and antisera
Workshop 10:
Local Production
  • 13:30 - 15:00
Coffee Break
  • 15:00 - 15:30
Plenary 3:
Access to Medical Products: CRP, FRP, Joint assessment procedures
  • 15:30 - 17:00
icdra Reception
  • 19:00 - 21:00

Please note that the agendas for Pre-icdra and icdra provide a draft outline of the event which will be updated regularly

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