Health Data for Research
Our solutions support research teams, trial sites and clinics in the efficient management, organization and execution of clinical trials –, compliant with applicable laws and guidelines.
Discover our solutions for research teams, trial centers, clinics
Our clinical research product suite includes specialized solutions that help trial sites, research institutions, and clinics conduct clinical trials efficiently and compliantly.
This includes TrialComplete – the clinical trial management system that accompanies the entire study life cycle from recruiting to study conduct, reporting and data export.
TrialComplete supports site operations for early (Phase I/IIa) and late (Phase IIb/III) or scientific / academic clinical trials in one portal and ensures GDPR, GxP, FDA and EMA compliant data processing:
TrialComplete EarlyPhase is tailored to meet the unique needs of the early phases of clinical drug trials (Phase I/IIa). The solution supports research teams and study sites in rapid subject enrolment, lab and device integration, and efficient control of complex study processes. With comprehensive interfaces and laboratory modules, TrialComplete EarlyPhase automates the entire study process with the extensive use of barcodes and scanners.
TrialComplete LatePhase is aimed at research teams that conduct academic and/or multicenter drug and device studies, especially those requiring the collection storage and processing of medical images. The platform enables the processing of large image datasets in DICOM format and ensures the highest level of data security and interoperability. The LatePhase version of TrialComplete facilitates the pseudonymized processing of study data and supports collaboration via interfaces to PACS and CDMS systems.
TrialSite, is a tailor-made solution for clinics that participate in clinical trials as trial sites. The platform enables systematic management of studies and documents, the automatic creation of study cost estimates and consistent billing of academic achievements. With the integration of AI-supported processes to automate administrative tasks, TrialSite optimizes efficiency and ensures legally compliant processes in accordance with the EU State Aid Act and the EMA guideline.
Finally, our Research Portal enables research institutions to easily access treatment data from CDR and IOP . It offers pseudonymized or anonymized data sets for internal and external research projects. A structured approval procedure protects patients' rights and accelerates research processes.
