Data is at the center of every successful regulatory submission. At Beaufort, we understand the value and significance of applying a data-centric approach to your clinical research program. Beaufort’s dedicated team of data science experts leverage decades of diagnostic and therapeutic experience to offer comprehensive data management and statistical services that can help speed your product to market.
Our integrated approach to data management and biostatistics is designed to seamlessly protect the integrity of your data, ensure quality and consistency throughout the entire clinical development process and support your product claims and overall strategy. We work in close collaboration to deliver insights to help you make smart and fast decisions that can mean all the difference in the success of your trial.
We also understand the importance of providing flexible and scalable solutions that match your project needs. Beaufort can be your full-service resource to deliver end-to-end clinical trial management services — or we can quickly and efficiently step in at any point during your trial process to support a specific data management or statistical need.
Clinical Data Management
Beaufort provides state-of-the-art data management services that maximizes quality, enhances data integrity and security, and improves overall trial efficiency.
Our highly-skilled biostatisticians translate your data into actionable insights — and support your team from protocol development through final analysis and reporting.