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Expert clinical biostatistics for optimized study design and executionThe i3 biometrics team delivers biostatistical programming and statistical analysis that is second to none. Our dedicated team leads us in evaluating our processes and tools from study design through regulatory submission, to ensure your study is executed as efficiently as possible and with the highest degree of quality to help you accelerate timelines and reduce costs. Our primary purpose is to get you your study results on time and on budget.The most direct routeWe’ll leverage our vast clinical experience to save you time and money, designing studies in a way that speeds submissions. We’ll reduce the need for retraining and increase the quality of service, and by applying previously established templates and communication pathways we’ll help reduce the duration of your project. Adaptive DesignWe’ve had good experience applying principles of adaptive study design, a methodology in which we evaluate trial results continually beginning in early stages, and modify study design parameters as required. Through this method’s continual course corrections, we’re able to help you save time to market, reduce costs, and help people live healthier lives. Data analysis Our many data analysis services include:
Statistical analysis and insight - Study design
- Adaptive design consulting and simulation support
- Program and protocol development
- Data safety and monitoring board management and support
- Regulatory submission report
Statistical programming - NDA-ready data listings
- Summary tables
- Statistical figures
- Integrated safety & efficacy network
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