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European Medicines Agency

2017年12月01日 (金) 午前 8:30 - 2017年12月01日 (金) 午後 5:00

30 Churchill Place, Canary Wharf, London, E14 5EU, United Kingdom

EMA/DIA EU Statistics Forum

Programme now available!

Session 3: Methods/Strength of Evidence - Part 2

Session Chair(s)

Hans Ulrich  Burger, PHD

Hans Ulrich Burger, PHD

Senior Director of Biostatistics

F. Hoffmann-La Roche Ltd., Switzerland

The totality of evidence into account in a systematic way for decision making at all stages of drug development will be discussed as well as innovative approaches to combine data from randomised trials and observational data.

Learning Objective : Participants will be able to will be able to compare and contrast new late-phase clinical trial designs. As a result, they will be able to design and formulate their Phase IIIb/IV clinical development plan more effectively.

Speaker(s)

Jonathan  Alsop, PHD

Recently Developed Designs of Late-Phase Clinical Trials

Jonathan Alsop, PHD

Numerus, United Kingdom

Director

Mario  Ouwens, PHD

Embedding Randomized Controlled Trials into Medical Practice

Mario Ouwens, PHD

Astrazeneca, Sweden

Statistical science director

Christoph  Gerlinger, MSC

Christoph Gerlinger, MSC

Bayer Pharma AG, Germany

Senior Director, Statistics

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