An additional registration fee is required for all preconference tutorials. Register today for this tutorial.
This tutorial is a combination of theory, guidelines, practical considerations, and real-life solutions for those working in the clinical development environment (pharmaceutical, biotech industry, or CRO). The instructors, with the use of a case study presentation, will provide a basic understanding of the underlying methodology and the current guidelines on safety data. Aspects of the planning of clinical trials as well as the problems and pitfalls during the analysis of safety data will be presented.
Who should attend?
- Discuss how to utilize guidelines and regulatory requirements for clinical trials;
- Describe ways to contribute to safety analysis plans;
- Discuss the statistical safety analysis process and pitfalls that could occur;Identify impact of benefit-risk assessment in safety data.