EDC On Demand

The business argument for EDC is well documented: Reduce your cost per page of data by as much as 80%; Lower overall clinical trial operating expenses by as much as 50%.  In short, make better decisions sooner and more cost-effectively.

But that’s only half the equation.  EDC must also meet the changing dynamics of an industry looking at new approaches to clinical trials and drug development.  Adaptive clinical trial designs, for example, are increasingly considered a viable alternative to the standard way studies are conducted.  To manage adaptive clinical trials, however, requires robust statistical applications and a real-time EDC environment.  Targeted or customized treatment solutions (TTSs) also require a technology infrastructure that can scale and manage a full range of complex analytical applications.  And internationally-administered clinical trials further heighten the need for data standards, such as those advocated by CDISC.

ClinicalAnalytics 4.0 delivers better study results faster, meets the business imperatives of lower operating costs and supports emerging ways to start and conduct studies.  As the industry’s first browser configurable on demand EDC solution, ClinicalAnalytics 4.0 enables you to flexibly create and manage different studies regardless of phase or therapeutic area.   And because it’s on demand, requiring only a Web browser to enter and manage data, ClinicalAnalytics 4.0 lets you deploy your studies twice as fast as more conventional EDC solutions, while readily scaling for globally managed trials and enterprise-wide deployments.  Here’s why:

  • Browser configurability to more effectively create study designs
  • User-friendly browser interface with drag and drop functionality
  • Integrated reporting
  • Real-time data management and analysis with audit trail management
  • Flexible data capture with image-based eCRFs and ePRO
  • Modular platform configuration to support the integration of strategic partners and custom applications
  • Extensive customer support and training
  • Compliance with GCP, 21 CFR Part 11 and other regulatory guidance
  • Support for CDISC standards

“Our customers can deploy ClinicalAnalytics 4.0 within two weeks compared to the industry average of 10.”  Jeff Smith, CEO and President, ALLPHASE Clinical Research

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