BatchLine was proud to participate in the ISPE Indonesia seminar, “Optimized & Compliant Digital Operations with EBR and eQMS,” where pharmaceutical industry professionals gathered to explore practical approaches to digital manufacturing, compliance, and operational excellence.
A key highlight of the event was the regulatory perspective shared by Dr. Shanti Marlina from Badan POM, who discussed the importance of digital systems in supporting GMP compliance, data integrity, and the future of pharmaceutical manufacturing in Indonesia.
During the seminar, Orchun Thakral, Head of Customer Success and Sales Director at BatchLine, presented
- Practical EBR implementation guidance Covering process mapping, User Requirements Specifications (URS), project planning, pilot strategies, vendor selection, and lessons learned from real-world deployments.
- Live BatchLine EBR demonstration Showcasing digital batch execution, review by exception, real-time production visibility, and audit-ready electronic batch records to support compliant manufacturing operations.
We would like to thank attendees who visited the BatchLine tabletop throughout the day. The strong interest in EBR, MES, and digital manufacturing highlights the growing momentum towards paperless and data-driven pharmaceutical operations across Indonesia.
Looking to start your EBR or MES Journey?
If you missed the session or did not have the opportunity to speak with our team during the event, we’d be happy to connect.
Contact us to learn how BatchLine can help you achieve compliant, efficient, and paperless manufacturing operations.
