We offer our clients comprehensive services associated with managing and processing of data in clinical trials, including creation and programming of databases, processing and verification of filled-in data, monitoring data, reporting of adverse events, statistical analysis plan (SAP), statistical analysis, preparing statistic report and final presentation of the study. To achieve this we use dedicated eCRF system developed by us.
At the request of the client we work in accordance with the standard operating procedures (SOP) specified by our client and requirements of Good Clinical Practice (GCP).
The integrated research platform – eCRF – enable us to collect, process and analyze valuable epidemiological data, resulting in unique and desired medical records. We consider ourselves as a reliable partner, to whom you may entrust development of medical record.
We comprehensively perform non-interventional observational studies, which are intended to collect scientific data and provide answers to research questions. We help our clients at every stage of the project, from the designing of the concept of the research and statistical analysis plan, through preparations of research materials and data collection process, to analysis of the results and preparation of final report.
We conduct our operations in accordance with the rules of Evidence Based Medicine (EBM).
