As a data-focused CRO, with strong programming skills, Quanticate has developed a range of solutions built on and around our iQ portal. In conjunction with our partnerships with key vendors in the Clinical Technology space, these enable innovative approach to clinical monitoring from a statistical perspective, collaboration on document development and easy access to data, documents and visualizations across studies. The complete trial life-cycle is covered, from planning, through monitoring, data capture, reporting and regulatory submissions. Our team has experience supporting many leading and niche technologies.
Risk Based Monitoring
The largest shift in methodology and process execution that the clinical trials industry has faced since the advent of electronic data collection.
Centralized Statistical Monitoring
Study design, protocol development and Statistical Analysis Plans (SAPs) that use a risk-based approach, as well as the creation, analysis and presentation of Statistical Monitoring Reports.
Traditionally much of the data within clinical trials is collected directly on paper and entered into an EDC, this process can be streamlined to enhance trial quality.
Results enables Clinical Operations staff or Clinical Data Managers to easily drill down into outliers and determine the corrective action required if any.