Speeding Clinical Trials with BIOVIA Pipeline Pilot

Automating and Standardizing Clinical Trial Data Management for Neurodegenerative Diseases


 

As a leader in development of therapeutics for neurodegenerative diseases, this BIOVIA customer was in need for a consistent and efficient way of managing clincial trial data.

Read this use case to discover how BIOVIA Pipeline Pilot helped:  

  • Save almost 40 years of FTE work for clinical trial data management
  • Increase in data Quality Control throughout
  • Shorten “database lock” time for FDA submission from 4 months to 2 days
  • Decrease variance in data quality across multiple sites
  • Improve processes through streamlined site-by-site investigation
  • Improve design visualization and communication.

Download the use case now!

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