Time

20 November 2019

(Wednesday)

09:00-10:30

Plenary Session 3

Leveraging Regulatory Networks for Access to Quality, Safe and Affordable Medical Products Including Digital Tools for Strengthening Regulatory Systems

10:30-10:45

Tea Break

10:45-12:15

Plenary Session 4

Smart Safety Surveillance for Strengthening Pharmacovigilance Systems- Progress Updates and Next Steps

12:15-13:30

Parallel Session 5

Moving Towards Smarter Clinical Trials– Changing the Paradigm in the Context of Global and Multi Regional Clinical Trials

12:15-13:30

Parallel Session 6

Medical Technology Pathways for Innovative Medical Devices

13:30-14:30

Lunch

14:30-16:00

Parallel Session 7

Medical Products for End game for HIV/AIDS, Tuberculosis, Malaria

14:30-16:00

Parallel Session 8

Global Partnerships for Drug Discovery, Innovation and Technology Development: Scaling up Adaptive Technology Solutions for Medical Products

16:00-16:15

Tea Break

16:15-17:30

Plenary Session 5

Re-purposing of Medicines for Reduced Approval Timeframe, Decreased Costs and Making Use of Existing Data, including issues related to Active Pharmaceutical Ingredients

16:15- 18.30

Workshop on Drug Development: Risk Assessment through Data Analytics

17:30-18:00

Wrap Up Plenary Session: Summary of the Plenary and Parallel Sessions