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.