Reduce Clinical Trial Delays and Improve Cross Study Performance

A Better Way to Track Clinical Trial Samples and Consents

In this whitepaper, we review the current challenges in tracking biospecimens and related consents in clinical trials, describe our unique approach for a novel informatics solution, and showcase real-world use cases from our current clients.

  • Improve sample collection operations
  • Resolve sample and consent issues earlier
  • Reduce lead time prior to interim analyses
  • Reduce database lock time

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