Learn How To Aggregate Data from Multiple Clinical Trials

posted on May 15th 2014 in Solutions with 0 Comments /


“Data” is the life science industry’s most valuable asset, and sponsors are searching for ways to leverage their clinical trial data to support critical decisions. This requires aggregate data from multiple trials be delivered in a concise, easy-to-use manner. Today, systems that support clinical trials are focused on collecting, cleaning, tracking, and analyzing data from individual trials.

This white paper provides insights into how sponsors can maximize the value of their clinical data with a clinical data repository.

Specifically, this data aggregation white paper provides:

  • How a CDR provides advanced analytics for actionable insights

  • The critical role a CDR plays in a successful risk-based monitoring approach

  • The opportunity to easily share data with partners and external collaborators

  • How a CDR supports efficient reporting to regulatory authorities

  • Best practices for implementing a CDR

  • A pharma case study on implementing a CDR

If you’d like a copy of the white paper titled “Data Driven Innovation through a Clinical Data Repository”, please click to download it.

Join the conversation and share your thoughts on this latest white paper. Have you thought about implementing a clinical data repository? If so, share with us why you are, or are not, moving forward with this initiative.

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