BatchLine is proud to participate in the upcoming ISPE Indonesia Annual Forum 2025, themed Adherence to Quality Compliance in Achieving Manufacturing Sustainability —a premier platform bringing together pharmaceutical industry leaders committed to advancing sustainable and compliant manufacturing.
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Featured presentation
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In this session, we’ll explore how digital quality systems, including eQMS (Electronic Quality Management Systems) and EBR (Electronic Batch Records), contribute to smarter, more sustainable, and more compliant pharmaceutical operations.
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Key Topics Include:
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1. Overview of eQMS and EBR in the Pharma Industry
- Core functionalities and compliance requirements
- Regulatory drivers (FDA 21 CFR Part 11, EU Annex 11, ICH Q10)
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2. Sustainability in Pharma: Current Landscape
- Green manufacturing and ESG expectations
- Defining sustainability in regulated environments
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3. Enabling Sustainability through eQMS
- Improving document control, training, CAPA, audits, and change control
- Case studies showcasing waste reduction and process efficiency
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4. Reducing Waste and Enhancing Efficiency with EBR
- Real-time batch monitoring and lean operations
- Enhancing right-first-time production and reducing rework
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5. Future Outlook: Digital Quality Systems for a Sustainable Future
- AI, predictive analytics, and smart compliance technologies
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Explore our solutions at Booth No. 3
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Visit us to experience live demos of BatchLine Lite MES, our innovative solution for digital batch records. Speak with our experts to learn how BatchLine helps pharmaceutical manufacturers:
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- Simplify compliance
- Eliminate paper-based processes
- Drive operational efficiency
- Support long-term sustainability
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We look forward to connecting with you in Jakarta to discuss how digital transformation can support your sustainability and compliance goals.
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Let’s Talk in Jakarta
