Bridging the Gap between Bio-Pharmaceuticals,
CROs, Clinical Investigators and Trial Participants

Study Data

One of the challenges in clinical trials is to ensure that all stakeholders have 24/7 access to all relevant Study information, including up-to-date information on Study Progress and other Key statistics.
Study-Portal can be configured to have a secure interface with your clinical data repository, thus allowing Study Metrics to be shared with all relevant parties. The integrated reporting and graphical tools allows for easy access to Study Metrics, ranging from Patient recruitment data to detailed information regarding the status of your Query or DCF process. By interfacing to your clinical DBMS, the Portal becomes a central place for all Trial participants to access key study information and documentation.

Dynamic content Filtering

Site information from your Clinical DBMS can be linked to the Portal’s User information, thus allowing to automatically filter information by Site-ID. As an example, when a Site request a report on Site performance, they will get a report based solely on their own data. While a Sponsor will be able to get a report over all Sites, or split-up by Site. Similar to any other module, any User will only see information and content which is relevant for their role in the clinical study.
Another example of this dynamic content filtering would be a patient survey using Quality of Life scales. You could allow patients to login to the Portal and get an overview of their individual Quality of Life scores over time.

Reporting and Graphical tools

Study-Portal is using an integrated Reporting tool, allowing to create reports and graphics for every purpose. A number of standard reports (e.g. patient and site overview) are available. New reports can be custom-designed on a Mac or Windows clients and can easily be integrated into the Study-Portal.