Collecting, managing, analyzing and submitting clinical trials may become a difficult task, especially when your trial has multiple sites, many patients, investigators, data managers and trial mangers. it turns to be even more complex when you have to comply with data security, regulations, interfacing with external sources and submission requirements. Introducing IEDC - Intelligent Electronic Dat
a Capture solutions We deliver intuitive, integrated and intelligent EDC solutions for all clinical study phases/ We will build with you the system all the way from the designing the study, the protocol, through the electronic Case Report Form, bio-statistician analyses, final medical report and submission. Together with our technology partners who lead the industry we offer the most advanced e-clinical ecosystems comprised on the best 'Plug and Play' components built for the job. You will be amazed how: • Your Data quality assured to be updated and edit checked preventing input of invalid or incomplete data • Patient compliance improved through a scheduler monitoring and reminding systems • You will achieve Maximum usability, better patient experience, better compliance and higher quality data • The Access to the collected data in real time allow truly adaptive studies • The system turns to be cost-efficient scale-ability, maintain know-how preservation, and has direct access to data gathered worldwide Don't wait any farther Time to get rid of papers and move to intelligent EDC solutions. Give us a call and we will be happy to demonstrate our capabilities.
