About This Case Study
Vector BioMed, a leading CDMO specializing in lentiviral vector manufacturing, successfully transitioned from paper-based batch records to a fully digital Electronic Batch Record (EBR) system using BatchLine Lite MES — all within just 4.5 months from project kickoff to full validation.
This rapid transformation showcases what’s possible when innovation meets execution in a highly regulated environment.
What This Case Study Reveals
- Digital Transformation Journey
How Vector BioMed transitioned from paper-based to fully digital workflows using BatchLine Lite MES to streamline GMP operations.
- Overcoming Challenges
Discover how iterative design sprints and qualification test runs helped tackle complex MBRs and ensure a smooth go-live.
- Implementation & Results
A deep dive into the fast-tracked 4.5-month implementation, including recipe design, CSV documentation, and hands-on team training.
- Actionable Insights
Practical lessons on early EBR adoption, managing process complexity, engaging end users, and running pilots before scaling.
Ready to dive deeper?
Download the full case study to discover how Vector BioMed accelerated digital transformation, improved operational efficiency, and achieved compliance with speed and confidence.
