Siris uses an eClinical software and service company dedicated to enabling our partners—pharmaceutical, biotechnology and contract research organizations—to bring new drugs to market faster and more efficiently. Our eClinical company offers fully integrated electronic data capture (EDC), interactive voice response (IVR), and electronic patient diaries (eDiaries).
We offer these products together in a fully-integrated platform or as individual technologies that collect, manage and analyze clinical data. We offer our customers unprecedented insight into all aspects of their clinical trial, maximizing their return on investment and accelerating their drug development timelines.
EDC
The EDC is a web-based, globally-proven solution for collecting, managing, and analyzing real-time clinical trial information. The EDC solution is used by pharmaceutical, biotechnology, medical device, and contract research organization customers around the world to enhance decision making and accelerate time to market. With configurable electronic case report forms (eCRF), study information is more accurate, timely, and accessible to the entire team for better collaboration and communication. The dynamic business process engine supports multiple workflows and ensures that information collected in the field is verified and complete. And real-time analytics support Adaptive Study designs by enabling better integration of study information and knowledge as the trial progresses.
eDiary
By using the eDiary to collect data electronically, sponsors can avoid the problems associated with paper-based collection such as patient compliance, transcription errors and limited data analysis. The ePRO solution features improved security and offers patients peace of mind in knowing that their sensitive data is protected. The eDiary provides interfaces that are simple to use for patients of all ages, from pediatric to geriatric populations; and makes collecting patient-compliant data easy.
IVR
The IVR is the only eClinical solution that offers patient enrollment, dynamic randomization, drug supply management and real-time analysis through one easy to use web-based interface. More than just IVR, the Web interface is a powerful trial monitoring and control tool. The IVR enables sponsors to easily manage site or stratum-based patient enrollment, the compliance of sites and subjects, and what supplies have shipped. IVR makes managing trials easy.
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