i-Monitor is an intelligent software engine & applications system, designed to monitor predominately Phase I clinical trials, but applicable to all clinical research activities and to fully comply with US FDA CFR 21 Chapter 11 regulations. This unique solution is built to satisfy the expectations of the highly regulated pharmaceutical industry. i-Monitor provides the features that are requested by the FDA to define, execute, track, audit and monitor studies based on industry standard protocols and regulations. i-Monitor will serve and facilitates all users involved in a clinical trials project. The i-Monitor automate the management of Phase I volunteers, data, samples and operational workflow. The i-Monitor suite consists of a series of modules to facilitate the rapid setup and running of Phase I clinical trials and the collection of key clinical trial data .
iMonitor is developed with the support of World Leading European CROs with more than 30 years of Clinical Trial Experience
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