It’s 2024, and in most clinical trials, data is still being moved from the EHR to the EDC manually – with employees reading data from one screen and typing it onto another. How did we get here?

[2] This is rather ironic, given that well-designed clinical trials should be amenable to very simple data handling and analysis. [3] Indeed the flowchart established by the CONSORT (Consolidated ...

In the dynamic environment of biotechnology trials, the significance of Clinical Data Management systems (CDMs) cannot be overstated. As we navigate the complexities of these trials and the ...

The solution is especially beneficial for organisations looking to “consolidate” sourcing efforts and minimise trial delay periods.