Plenary 1:Smart Safety Surveillance – a shared responsibility: moderated panel discussion.
Plenary 2:Regulatory collaboration, convergence and harmonization: “transfer” of regulatory information.
Workshop 1:Regulatory preparedness for public health emergencies.
Workshop 2:Certification of Pharmaceutical Products: is it still “fit for purpose” in a modern environment?
Workshop 3:Global Benchmarking of Regulatory Systems: from individual countries to networks.
Workshop 4:Risk-based inspections: potential for work-sharing.
Pre-ICDRA Welcome Reception
Please note that the agenda for Pre ICDRA and ICDRA provide a draft outline of the event which will be updated regularlyDownload Schedule
Workshop 5:Enabling access to innovative medical products in resource-limited settings.
Workshop 6:Changing procurement models: maintaining safety and quality of medical products.
Workshop 7:Local production of medical products: regulators’ role.
Workshop 8:Regulation of advanced therapies.
Workshop 9:Progress in regulation of medical devices (including IVDs).
Workshop 10:Regulation of biosimilars.
Plenary 3:Partnerships to enhance better regulatory outcome.
ICDRA Welcome Reception
Please note that the agenda for Pre ICDRA and ICDRA provide a draft outline of the event which will be updated regularly