Imaging in clinical trials has seen tremendous growth over the past two decades and is increasingly used as the primary endpoint for some related trials. However, variability across images collected (and subsequent analysis) inevitably leads to larger sample sizes, longer timelines and bigger budgets, putting added pressure on study teams to minimize these risks. In this Best Practices Guide, get practical strategies for how to successfully:

  • Enable more objective assessments unencumbered by reader bias
  • Streamline regulatory compliance and speed approval timelines
  • Achieve greater data consistency and complete data transparency
  • Reduce rework and drive operational efficiencies

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