Transitioning to Digital Work Instructions
Client: Global Japanese pharmaceutical company – European lab environment
The Challenges
Laboratory processes relied on printed Word-based forms, filled in by hand—error-prone, hard to analyze, and unscalable. The goal: establish a fully digital, GxP-compliant, 21 CFR Part 11–compliant system.
The Solution
The Result
All data entry is now carried out via tablets. The final PDF files include a complete audit trail with timestamps and user actions. The customer benefits from a fully digital, standardized, and highly automated laboratory process chain that significantly enhances data access, traceability, and data availability for analytics and AI evaluations.