Writing Clinical Trials To The WebvTrialsPlus clinical documentation and monitoring solution simplifies data acquisition and monitoring through use of Anoto Digital Pen and Paper (DPP). Benefits include
How It Works - Schedule A DemoDPP renders source information handwritten on CRFs into digital format instantly. The information is then securely uploaded to a web portal for viewing, analyzing, and coding by authorized personnel. If you choose to use the XML stream, the data can be applied without rekeying or scanning. Intuitive Data Acquisition
The efficient and intuitive acquisition of data from the digital pen provides clinicians and researchers with an easily adopted EDC solution. Unlike other devices, the digital pen does not require changes in process or extensive training. It also does not interfere with the patient-doctor interaction. The digital pen has proven in research studies to be the fastest and most accurate form of mobile data entry. Immediate Data Availability
As the clinician finishes an interview with the patient, a simple stroke of the pen across the "send" box beams the data to a cell phone that uploads the clinical report forms to the research organizations web portal. Authorized personnel can immediately monitor and verify the data. Custom alerts can be programmed to notify clinical trial monitors of uploaded CRFs, adverse events, or incomplete forms. This real-time interaction between the site and the monitor can reduce errors, save travel time, and bring products to market faster. Click here to read how vTrialsPlus reduced travel and monitoring time for Coherex Medical. Complete VisibilityvTrialsPlus provides a complete audit trail of CRFs with a date/time stamp for all entered data. Velosum's proprietary software provides clients with three forms of the data: the full rendered CRFs as they were written for compliance with FDA regulations, translated CRFs for easy monitoring, and XML data for input into clinical trial databases. Database Integration
Velosum works with the clients IT staff to seamlessly integrate the data captured from remote sites into the organizations clinical trial databases for immediate analysis. This benefits our clients by eliminating the delays caused by additional processes of rekeying or scanning CRFs and can reduce the time of a clinical trial. |
