C&Q Guide (third edition) – what’s new and what truly matters?
This session provides a detailed overview of the most important updates introduced in the third edition of the C&Q Guide. We will explore which changes have a direct impact on the qualification process, how they are positioned from a regulatory standpoint, and what practical implications they hold for day-to-day work in GMP-regulated manufacturing environments.

Qualification of water systems – common pitfalls and proven best practices
We will examine the typical challenges that arise during the design, qualification, and ongoing operation of modern pharmaceutical water supply systems. In addition, we will outline best practices that help minimize risks—from microbiological control and documentation requirements to preventive measures that support long-term system reliability.

Life-cycle approach & change management – sustainable strategies for GMP-compliant systems
This section explains how a comprehensive life-cycle approach enables efficient, compliant, and future-proof system operation. It also highlights how structured, well-documented change management ensures that modifications are implemented in a controlled, transparent, and regulatorily sound manner.

Following the presentations:
A panel discussion with experts from industry and consulting. Your questions, your topics, your stage—an open forum to address specific issues and develop practical solution approaches together.