Asset performance management – beyond the software
Wood has an extensive background in applying regulatory requirements, expectations, and standards on all projects. We provide the full gamut of CQV service offerings from conceptual design through handover and ongoing qualification and validation maintenance.
Our CQV team works closely with engineering, manufacturing, procurement, quality systems, and construction to ensure quality is embedded in the project, user requirements are achieved in the design, regulatory concerns are addressed, and commissioning, and qualification needs are clearly communicated to the entire project team.
We make it a priority to stay aligned with current pharmaceutical regulations, guidelines and client requirements and address them throughout design, construction and CQ phases. Using regular, formal current good manufacturing practice (cGMP) reviews, we document our compliance and prepare to defend regulatory agency submissions and inspections.
Early involvement of our CQV team ensures a smooth transition throughout each project phase. We follow the life cycle approach to commissioning, qualification and validation to define requirements during the earliest project phases, allow for a staged approach to qualification and achieve the best value.
Beginning with the end in mind, our team of experts are here to deliver the most complex Life Science projects. From strategy and design, through construction, start-up and CQV, we apply our expertise using the latest digital tools and lean delivery concepts to bring the best value and solutions to our clients.
Achieving upside outcomes – CMMS migration and data optimisation
Helping to offset the CO2 in the era of aging infrastructure
Learn how to find and solve vibration problems in piping systems. We'll show you new ways to identify vibratory service and examine the strengths of this test