Thank you to everyone who visited us at ISPE Indonesia Annual Forum 2025, where we proudly showcased BatchLine Lite MES—our smart, compliant, and affordable Electronic Batch Record (EBR) and Lite MES solutions designed for GMP-regulated manufacturing.
The event’s theme, “Adherence to Quality Compliance in Achieving Manufacturing Sustainability,” aligned perfectly with BatchLine’s mission to help pharmaceutical manufacturers reduce paper-based inefficiencies, enhance data integrity, and support sustainable operations through digital transformation.
Presentation Highlight
“How eQMS and EBR Support Sustainable Pharma Operations”
Presented by Chompunut Apinan, Project Manager
In this insightful session, Chompunut explored how implementing eQMS and EBR helps pharmaceutical companies reduce waste, improve data integrity, and streamline operations—all while supporting their sustainability and compliance objectives. The session sparked great discussions and highlighted practical examples of digital systems driving measurable improvements in pharma manufacturing.
At the Booth
At our booth, attendees experienced how BatchLine Lite MES is helping GMP manufacturers:
- Accelerating batch review and approval times
- Simplifying implementation and validation
- Enhancing compliance and operational visibility
- Reducing waste and improving right-first-time production
We appreciated the opportunity to connect with industry professionals, share success stories, and demonstrate how BatchLine is enabling real, measurable improvements for pharma companies.
Let’s Continue the Conversation
Interested in how BatchLine Lite MES can help your organization drive efficiency and sustainability?
