Case Study: CIDP improves clinical trial data quality and efficiency with Datacapt

CIDP saves 40% of data management time with Datacapt

CIDP, an international CRO, faced challenges in managing global clinical trials with a paper-based system reliant on spreadsheets. This process required double data entry, complex quality controls, and tedious query clarifications, hindering efficiency and data integrity. As part of its digitalization ambitions, CIDP sought a cost-efficient, robust, and remote-friendly tool to elevate its data standards and meet sustainability goals.

CIDP implemented Datacapt, an integrated platform featuring eCRF, ePRO, and eConsent modules. The solution centralized data collection, provided real-time sponsor access, and ensured compliance with international regulations. Datacapt helped CIDP save 40% in time spent on data management, achieve cleaner data at the source, and offer a more environment-friendly solution. The transition was warmly welcomed by staff and patients, with the tool providing growth opportunities for team members and streamlining the entire clinical trial process.

CIDP