Innovative Approach to Annual Product Quality Review Creation
A biopharma drug manufacturer needed to integrate data from diverse sources; keep up with the continually evolving regulatory requirements; maintain accuracy while meeting deadlines, as well collaborate and communicate more efficiently across departments.
The customer leveraged BIOVIA Structured Document Authoring – APQR along with BIOVIA Pipeline Pilot, for docment initialization and BIOVIA Discoverant for data integration and statistical process control.
Download the use case to learn how this powerful trio of BIOVIA solutions reduced the customer’s root cause investigation process from one month to one hour, expediting time-to-market for its products.