Seminar

Every pharmaceutical product carries an implicit promise: quality, consistency, and safety. That promise is upheld through confidence in development and quality control. As manufacturing scales and regulatory expectations continue to evolve, labs are under increasing pressure to generate reliable, compliant, and release-ready data faster than ever before. With Vietnam's pharmaceutical industry accelerating its ambitions for global market access, aligning with international quality standards such as EU-GMP has become an increasingly important step toward strengthening manufacturing excellence and competitiveness.

Yet many laboratories still operate through fragmented workflows, where manual processes and disconnected systems limit efficiency, delay decision-making, and increase compliance risk. A more connected approach is now essential.

This seminar brings together industry and Agilent experts to explore EU-GMP expectations, opportunities for Vietnam Pharma, and implementation experiences, alongside analytical workflows and digital integration strategies for future-ready QC labs. Through practical, application-driven discussions, attendees will discover modern approaches to impurity and nitrosamine analysis, real-time material verification, and digitally enabled QC workflows that enable faster, more confident decisions.

What You'll Experience?

• EU-GMP Readiness & Manufacturing Excellence - Gain valuable insights into evolving EU-GMP expectations, opportunities and challenges for Vietnam's pharmaceutical manufacturers, and practical implementation experiences from EU-GMP manufacturing facilities to support global competitiveness.
• Connected Analytical Workflows - See how modern LC and LC/MS workflows improve throughput while maintaining consistency, robustness, and control across routine QC operations.
• Digital Integration & Data Integrity - Explore how integrated informatics platforms enable seamless data flow, strengthen data integrity, support regulatory compliance, and reduce reliance on manual processes.
• Advanced Approaches to Impurity & Contaminant Analysis - Discover practical analytical strategies for addressing emerging challenges such as nitrosamines, extractables and leachables and other complex impurities with greater confidence.