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Final Programme - iuphar

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FC07 Simulation and data modelling in drug development.<br />

Better drugs faster?<br />

Leaders: Hartmut Derendorf, (USA)<br />

FC07.4 Modelling and simulation – a regulator’s view<br />

Jogarao VS Gobburu, (USA) & Hartmut Derendorf, (USA)<br />

14:30 - 14:55 FC07.4.1 Role of modelling and simulation at the FDA<br />

Jogarao VS Gobburu, (USA)<br />

14:55 - 15:20 FC07.4.2 Role of modelling and simulation at the European Medicines Agency<br />

Franz König, (UK)<br />

15:20 - 15:45 FC07.4.3 Role of modelling and simulation for drug approval in Asia<br />

Yuki Ando, (Japan)<br />

15:45 - 16:15 COFFEE BREAK<br />

16:15 - 16:40 FC07.4.4 Exposure-response and disease modelling from a regulatory view<br />

Siv Jönsson, (Sweden), A Henningsson<br />

16:40 - 16:55 FC07.4.5 Free Communication Presentation:<br />

Bridging preclinical and clinical data using a population-based simulation software<br />

Frank Larsen, (Denmark), KG Jensen, KB Petersen<br />

16:55 - 17:10 General discussion<br />

Tuesday 20 July ■ 14:30 - 17:15 ■ Meeting Room 18/19 87

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