Collaboration on documents and distribution of information across a clinical development program for a new product has never been so easy. iQ brings together data, information, knowledge and documents from disparate systems, presented in easy-to-use interfaces, with timely reminders and updates. Through this common platform, you can find the information you need, and get real-time access to the data and knowledge needed to enable faster decisions and optimal commercialization.
The iQ portal brings together the data, information, and knowledge generated in the development lifecycle of the clinical trial process. The dashboards and visualizations provide fast access to key data and information, from pre-defined and bespoke reports, helping you find meaning and knowledge from your disparate raw data.
Document development and review within a version-controlled environment provides a lean approach to your clinical trial process. Workflows model business and regulatory processes, delivering controlled approvals and reviews with timely reminders.
The iQ portal provides trial progress, quality and cost reports. Detailed graphical representation can then be drilled down and filtered when the user requires to enable fast decisions.
iQ offers a standard suite of Tables, Listings and Figures (TLFs) at no additional cost. These near-real time reports permit customers to review the progress of their study in advance of database close, allowing project teams to take a step back from the data and view the trial as a whole. These standard TLFs cover most major interests across study areas; additional custom reports are available for a small charge. Reports include; Demographics, Medical History, Prior Medications, Concomitant Medications, Adverse Events and Vital Signs.
Using a business intelligence tool to manage the information process flow provides you with reliable access, traceable processes, and single trial or pooled product data to deliver fast answers through: