Records and Information Management

Life Sciences

Managing some of her medical duties

Records and Information Management

Life Sciences

Facilitate reviews and approvals, and maintain compliance, with our solutions for tracking and managing clinical trial data.

Bring it all together

For a clinical trial to run smoothly and successfully, trial data needs to be captured, organized and made readily accessible for doctors, researchers and reviewers.

This is easier said than done.  During the various stages, clinical trials generate massive amounts of physical and electronic information.

Improve your clinical trial process with the experts at TAB

  • track trial information in any format using TAB FusionRMS, our clinical data management software
  • collect and manage data throughout the trial stages, including registration, IND application, research and testing, NDA / BLA applications, review and approvals, results reporting and data sharing
  • facilitate FDA review and approval by keeping data well organized and easy to share, using biopharma industry best practices
  • avoid penalties and maintain compliance with requirements for clinical trial reporting
  • achieve data transparency commitments during and after the trial
Eight awesome ways that metadata supercharges your RIM software

Eight Awesome Ways that Meta Data Supercharges your RIM Software

Metadata plays an integral role in the success of software systems, and this is especially true with records and information management (RIM) software.

Unfortunately, many business professionals are unclear on the role of metadata and why it is so important for RIM systems.

This guide can help. It offers essential information for organizations thinking about implementing a RIM system, and those that want to get more from their existing system.

Download White Paper

Learn more about clinical trial solutions powered by TAB FusionRMS

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