Date/Time
Date(s) - April 14, 2026
8:30 am - 4:15 pm
Location
Hotel Morazen
Categories
In the evolving landscape of pharmaceutical manufacturing, the integrity of a single Chromatographic result rests on two inseparable pillars – the physical health of the analytical instrument and the robustness of the digital ecosystem governing it. For QC labs, the transition from “functional” to “compliant” is increasingly complex as regulatory bodies place higher scrutiny on instrument and data integrity and audit readiness.
This seminar provides a comprehensive roadmap for lab users and management to mitigate operational and regulatory risks. We will explore the digital frontier, discussing the necessity of timely software upgrades, the structured approach of CSV and the deployment of new software features specifically designed to automate compliance.
Key Takeaways:
- Identifying and closing gaps in legacy software environments
- Reducing audit risk through modern CSV practices
- Leveraging new software capabilities to mitigate data integrity risk
Date & Time:
🗓️: 14 April 2026
🕒: 08.30 – 16.15 WIB
📍: Morazen Hotel Surabaya
Speakers & Topics:
- Jeevetha Mali Waters APAC Principal Validation Informatics Consultant
“Audit-Ready and Empowered: Key Documentation Requirements for Empower CDS Validation”
- Alyssa Loo – Business Development Specialist at Waters Pacific
“Your Trusted Lab Partner: Navigating Data Integrity with Waters Informatics Solution”
- Songye Ho – Service Business Development Specialist, SEA, Waters Pacific Pte Ltd
“Empower CDS Lifecycle: The Path to Staying Current”
- Fauzan Moktar – Regional Service Leader ASEAN
“Smart Services: Leveraging Informatics for Operational Success”
- M. Zaqy Arif – Marketing Manager For Chem & Service Business PT Kromtekindo Utama
“Waters Informatics Update”
Please visit the following link to register: ➡️ https://forms.gle/WoPG5G8A8uUdHYaG9
Best regards,
PT Kromtekindo Utama