Developing the strategies to ensure efficient, compliant and time-saving progress in the clinical trials process

16 industry representatives, including 8 directors will join with 3 prominent academics to share their insights on how to:

• Understand adaptive trials and the best-practice implementation of adaptive methods in your clinical trials design
• Utilise Bayesian statistics to inform good decision making in the clinical trials process
• Unravel the problem of missing data and how best to deal with it in the course of your clinical trials
• Improve your meta analysis using Bayesian statistics and indirect comparison
• Facilitate dose finding in Phase I using adaptive trial elements (linked to Conference Day One 09.55 session]
• Recognise the opportunities and challenges of using biomarkers in the early development stages of clinical trials
• How to improve the reporting of you safety data using innovative graphical techniques
• Make use of simulation and modelling as innovative tools to enhance and improve the design and analysis of your clinical trials
• The future of statistical standardisation: moving towards a global alignment for statistical reporting
• Appreciate the importance of translational science in optimising your clinical trials processes

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