Agilent Seminar Modernizing Pharma Development and Quality through Automation & Innovation

As pharmaceutical products grow more complex, analytical and QC laboratories are under increasing pressure to deliver speed, consistency, and compliance - simultaneously. Intelligent automation, digitalization, and advanced analytical technologies are transforming how labs operate by connecting data, streamlining workflows, and embedding Quality by Design across the lifecycle.

To support this shift, we invite you to a focused, technical seminar designed to help analytical and QC teams respond to rising complexity and regulatory expectations with confidence.

Why Attend this Seminar?

• Regulatory-aligned updates: Stay current with Schedule M requirements and evolving QC expectations
• Practical, workflow-led learning: Real examples spanning raw materials, development, and final product testing
• Modern QC perspectives: How leading labs are adopting automation, digital tools, and advanced analytics
• Expert-led discussions: Learn directly from specialists across chromatography, mass spectrometry, spectroscopy, and compliance services
• Relevant for growing labs: Designed for organizations scaling operations while managing compliance pressure

The Outcome: Accelerated development timelines, stronger compliance, and more resilient, future-ready laboratories

👉Register now

Agenda

9:10 AM Welcome Address 

9:15 AM Agilent & You: Partnering for Analytical Excellence 

9:30 AM Complying to schedule M requirements with latest updates

10:00 AM Stay ahead with innovation- Tech Upgrade for Peak Productivity 

10:15 AM Accelerate productivity to multifold by leveraging method modernization in chromatography 

10:45 AM Impurity Profiling and quantification workflows with mass spectrometry solutions across the pharma value chain 

11:45 AM Tea/ Coffee Break 

12:00 PM Streamlining Laboratory Operations for Maximum Efficiency Optimizing workflows, reducing bottlenecks, and leveraging Agilent CrossLab services 

12:30 PM Automation & Digitalization - exponential growth strategies for Pharma Development Quality Control - Challenges & solutions 

1:00 PM Lunch 

2:00 PM Productivity, safety of the lab through right supplies & newer chemistries 

2:30 PM Development in Glycol and residual solvent - Explore what's latest thing in it? 

3:00 PM From Raw Material testing to Final Formulation-Identification & Quantification studies using modern spectroscopy solutions 

3:30 PM Q&A with Panel 

4:00 PM Thank you & Hi- Tea