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| Invision Innovative Technology Solutions |
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INVISION is a group of highly skilled engineers, scientists and health professionals with over 25 years experience developing technology based solutions for a wide range of companies in the Health and Life Sciences sector.
For the past three years they have been developing EVADO Clinical Trials Management Software.
EVADO by INVISION is a cost effective, intuitive web-based eCRF application that replaces paper-based systems. EVADO is suitable for trials in all phases and disciplines. EVADO can securely store data for between 1 and 20,000 trials making it ideal for all clinical trial situations. EVADO is powerful system that can support between 1 and 500 concurrent users. Built on the Microsoft .NET 2 platform, EVADO makes the creation of eCRF's simple. Online data entry results in 60% improvement in data quality due to reduced transcription errors. Anomalies are flagged and researchers are notified early of potential problems.
EVADO is available in a variety of configurations to suit all requirements from single-centre trials to world-wide trials.
Busines opportunities exist for Clinical Research Organisations, Pharma, Biotech or Device manufacturers, data management partners and research institutes who are interested in implementing web-based user friendly eCRF technology for their own organization/s and or their clients.
INVISION is also seeking sales and implementation partners who can support EVADO in the international Life Sciences sector.
EVADO is built on the Microsoft .Net 2.0 Framework. Mobile data entry is also possible with a tablet version due for release Quarter 3 2007 and an HL7 interface is currently under development.
EVADO Pre-Clinical module: is a customized version of EVADO specifically designed for collecting laboratory, animal and first human study information.
EVADO HL7 interface allows medical based research organizations to access patient medical information.
- Minimises the cost of ownership and simplifies deployment.
- Eliminates the need to create specific databases for each trial.
- Trial specific forms do not need to be laid out.
- Increases data accuracy by 60%.
- Collects trial safety data on-line, saving at least 1/2 day of manual processing each week.
- Eliminates double handling by automating CRF administration.
- Makes the running of either single centre or world wide trials economical by utilising the latest web technology.
- Process automation minimises trial administrative tasks.
- Stores the data from 1 to 20,000 trials.
- Manages between 1 and 500 concurrent users.
- Easy to use and can be learnt in one to two days.
- Installed once regardless of the number of trials that are initiated and run.
- Integrates easily with other external software packages.
- Provides comprehensive audit trails for regulatory compliance.
- Subject visits can be tracked and booked on line.
www.evado.com.au
 
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