Engineering Quality: A Journey Through URS and Risk Management

URS & Risk Assessment: The Foundation for Successful Engineering

A well-defined User Requirements Specification (URS) and a thorough Risk Assessment form the foundation of successful projects within the pharmaceutical industry. But how can you ensure that requirements, engineering, and quality are aligned from the very beginning?

During this event, organised as a collaboration between the CQV Community of Practice and the Quality Community of Practice of ISPE, we will explore the connection between engineering, quality, and risk management.

The event will focus on the practical application of developing an effective URS and performing risk assessments within pharmaceutical projects. We will discuss how a risk-based approach can support better decision-making, create clearer requirements, and contribute to more efficient engineering and quality processes.

This event is aimed at professionals at all levels working in the pharmaceutical industry who have an interest in engineering, quality, commissioning & qualification, validation, and risk assessments. It provides an excellent opportunity to exchange knowledge and experiences and to bring together different perspectives from both engineering and quality.

Join us for an inspiring and interactive event where practical experience, knowledge sharing, and collaboration take centre stage.