Key components of a central imaging workflow
Our team provides expertise on your imaging protocol design and tailors the reading scheme to your specific imaging endpoints. We will work with you on the following key documents:
Central imaging reader group
Accurate imaging starts with the right reading criteria
We have supported over 350 imaging studies, many in oncology—including pivotal trials—giving us extensive expertise in the following reading criteria:
We leverage our expertise to guide sponsors in selecting and implementing the most effective criteria to ensure high-quality, consistent data that supports confident decision-making.
Choosing the right image modality is crucial for achieving trial objectives
We can help you with trials involving all imaging modalities including:
We collaborate closely with clinical teams during the protocol definition phase to ensure that all imaging challenges are addressed.
Why is central imaging important in clinical trials?
Central imaging is crucial in clinical trials as it ensures consistency in image acquisition and interpretation across multiple sites. By standardizing processes, it reduces variability, minimizes reader bias, and enhances data quality.
This approach improves the reliability of imaging endpoints, making them more robust for statistical analysis. Moreover, central imaging plays a key role in supporting regulatory submissions by ensuring the integrity, accuracy, and traceability of data.
With a centralized system, you can confidently present consistent, high-quality imaging results that meet the stringent requirements of regulatory authorities.
