The percentage of eClinical trials within the global study market is growing rapidly in accordance with technological development. And for good reasons - because today, the potential of the underlying software by far exceeds mere data collection via the Internet. Ideally, EDC software acts as the heart of an eClinical platform. By mapping regulatory, medical, statistical and, last but not least, also time and financial requirements to study processes, this platform oversees the interactions of the study personnel involved and enables complete transparency and manageability of the project. These are features indispensable for every organization conducting clinical research.

As an eClinical solution, clinIT’s software TRI@L-IT serves you

• as a fast and efficient introduction to eClinical trials
• in collecting data and verifying them both online and offline by query management, source data verification and medical review
• in supporting project management by providing customized reports about the study conduct and by making all required documents available to the personnel involved
• in collecting and managing local laboratory normal ranges and integrating external data sources (central laboratory, ePRO, telemedicine)
• in performing hybrid studies that combine paper and electronic CRFs

Based on the detailed schedule of assessments, the automatic development process of TRI@L-IT allows immediate generation of the functional modules required for the relevant clinical project or program. Maintenance of cross-study standards enables both data transfer in definable common formats, e. g. CDISC, and re-utilization of data in meta analyses.

Above and beyond the features you might expect in any state-of-the-art EDC software, e. g. complete regulatory compliance, clinIT’s TRI@L-IT excels through its simple and easy-to-learn usability and its very fast system reaction times - even and especially in worldwide deployment. Our clients confirm TRI@L-IT’s excellence through regular client satisfaction surveys.