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replace traditional labour-intensive data collection
improve data quality
incentivise clinicians to collect data with value-added tools
With several years experience in medical outcomes systems, we can provide software which meets the particular requirements of clinical research studies, from post-marketing to regulatory and HIPAA compliancy. Systems can include support for tools such as patient-scheduling, double-data entry, anonymisation, printing case report forms, in addition to customisable reports. Such value-added tools further incentivise clinicians to collect data.
You may be supporting a multi-centre study, where traditionally data has been collected via paper CRFs before being collected and entered centrally. This is labour-intensive and not easily scalable, and often query-resolution caused by incomplete or incorrectly completed CRFs is very time consuming. With highly scalable distributed software or web-based outcomes systems, data is verified and validated at source and the clinician made immediately aware of any problems. In many geographical markets today verifiably high clinical data quality is seen as increasingly important and we can assist you in maximising the value of this research, while consigning traditional labour-intensive approaches to the past.