iQ - Integrated Quanticate

Optimizing the Organisational Performance of the Clinical Trial Process

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.


Intelligence Portal

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.

Collaboration and Workflow

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. 

Dashboard and Visualizations 

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.

Tables, Listings and Figures

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.

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System Features 

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:

  •  Easy to view data from multiple sources in a standardized format
  •  Full study documentation management and storage including version control
  •  Task notification for study deliverables and document reviews/approves 
  •  Customized notifications via portal or email
  •  Shared calendars and discussion forums for a global collaboration
  •  All content delivered via the portal are available on tablet, PC desktop, and laptop
  •  Automatic Metadata generation to classify content 
  • Customizable tags to categorise and search different documents, including both structured and folksonomy tagging
  • Global search functionality that reads all documents types including PDFs and all common Office documents
  • Gantt Chart views for of project plans, task tracking and resource allocation on your study

     

Security and Control

  • Logon access control across all related systems
  • Automated audit administration and easy reporting
  • 21CFR Part11 compliance
  • Document development and review controls
  • Check-in and check-out functionality
  • Shared access rules with the data and content store
  • Controlled access based on role or group

 

IQ Walkthrough