Risk analysis is a critical part of the design, implementation and assessment of medical research and healthcare provision and development. It plays an active role from the design of clinical trials in drug development through to post-marketing surveillance of outcomes, and to the assessment of risk to health from environmental, occupational and individual-specific factors.
The workshop will address aspects of quantification and mitigation of risk in health sciences. Different themes will include the modeling and analysis of occupational and environmental health, mitigation of risk in the context of infectious diseases, risk assessment in trial design for toxicity and efficacy in Phase II/III clinical trials, and the quantification of adverse event risk in post-market surveillance. Statistical methods which will be discussed in this context include spatial and causal modeling, clinical trial design and personalized treatment strategies.
Students and postdoctoral fellows are encouraged to present a poster at the workshop. One poster session has been scheduled, with a short lightning talk, so that trainees can introduce themselves and their work to the entire audience.