All data. Anytime. Anywhere
Trial leader, CRO, CRA, study centers and even (optionally) subjects, all can log on to their own section of the clinical trial website. If you log on as trial leader or CRO, you can manage iModems and medical equipment and manage your study centers and subjects. Being a investigator your access is limited to your equipment and subjects. Together with (optional) subject access the website has been designed to shape itself to your trial.
A perfect match
Combine the iModem with the Clinical trial website and you will have more power. With optimal support of the data-flows in focus, together with partners and clients the clinical trial website has been developed and perfected over the course of many years. It has a level of quality that lets you quickly implement the technology in your study design.
Good Clinical Practice, audit trail quality and other relevant issues are handled carefully and effectively by the system. From the selected medical equipment, the iModem, the ROS platform and the clinical trial website; all elements of the path that the data follows is designed to withstand any auditor.
To see a full features list, look at the features page.