Modernising pharma QA/QC laboratories: preparing for a more connected, compliant future

Pharmaceutical QA/QC laboratories are under increasing pressure to improve efficiency, maintain compliance, ensure data integrity and support growing operational demands, all while managing legacy systems, disconnected workflows and increasing validation requirements.

In this webinar, industry experts will explore what defines a modern laboratory informatics environment and why connected, standardised platforms are becoming the foundation of future-ready QA/QC operations.

Attendees will gain practical insight into the implementation, validation, integration and organisational change considerations that influence successful modernisation initiatives, along with a framework for planning an informatics roadmap that delivers both immediate operational improvements and long-term business value.

Whether you’re assessing legacy systems or planning your next phase of digital transformation, this session will provide a practical framework for understanding what a modern laboratory informatics environment looks like and how to confidently prepare your laboratory for greater operational consistency, compliance and future adaptability.

Key learning points

• Understand the primary operational and regulatory challenges facing modern Pharma QA/QC laboratories
• Learn how standardised laboratory workflows can improve consistency, efficiency, and compliance
• Explore how connected laboratory data and integrated workflows support more efficient, compliant and informed laboratory operations
• Discover strategies for reducing manual effort while supporting data integrity and controlled laboratory execution
• Understand the key considerations for planning modernisation, including implementation confidence, validation and long-term supportability
• Identify best practices for building a scalable, future-ready laboratory informatics environment that supports long-term operational excellence.