One of the fastest growing segments of the electronic clinical trial (ECT) market is electronic patient reported outcomes (ePRO). The adoption of electronic clinical trial technology has grown rapidly over the last few years as clinical trial leaders see new ways to streamline the drug development process while improving data quality and maintaining the highest levels of patient safety and compliance. ePRO solutions permit reports to be sent to the study team in real time, with faster validation and avoiding the loss of data in transit as well as eliminating human errors that occurs when trying to interpret handwritten answers.
According to the individual customer project requirements, CROS NT offers multiple technologies services for all PRO data collection allowing companies to improve efficiency, speed and accuracy of data at reasonable costs.
CROS NT has a fully validated and integrated ePRO solutions for Oracle Clinical RDC, which has successfully supported over 2000 patients in 175 sites. Integrating the ePRO with Oracle RDC helps the investigator in the day to day activities by accessing the RDC application on-line and displaying both the ePRO and the eCRF data.
Within RDC ePRO, data is stored in an encrypted mode preventing data from being changed, deleted or modified by investigators or patients. Data is securely transferred via HTTPS and delivered to CROS NT’s state of the art data centre. All services are available 24/7/365, with robust back-up and disaster recovery plans to provide confidence and reliability to our customers.
