
Blog
Which energy recovery system is right for my laboratory?
Laboratories and cleanrooms are among the most intricate and essential facilities within modern research and healthcare infrastructures. Ensuring these facilities maintain regulatory compliance from the start and throughout their operational lifespan is critical for their safety and effectiveness.
Wood has supported several private and public customers, including universities, healthcare facilities and research institutes, in optimising the performance and compliance of their assets. These projects range from Biosafety Level 2 (BSL2), Physical Containment Level 2 (PC2) and Biosafety Level 3 (BSL3), Physical Containment Level 3 (PC3) laboratories to complex plant greenhouse facilities and high-end cleanrooms.
Through our involvement in these projects, we have developed a unique approach to complex facility operational commissioning and handover. Enhanced commissioning, verification and post occupancy optimisation are three pivotal elements of our approach which underpin laboratory safety, facility effectiveness and compliance.
Enhanced commissioning is a significant evolution from traditional commissioning practices. It goes beyond basic commissioning requirements ensuring that building systems are constructed, tested and commissioned as designed. It includes actions like detailed system integration testing, cross-system dependency verification, interface testing between different systems and failure mode analysis and recovery testing.
The goals of enhanced commissioning extend beyond mere functionality, confirming system performance under various conditions. This results in optimised operational efficiency, improved energy use and improved long-term reliability through failure prevention strategies and consistent performance. Examples of enhanced commissioning for BSL3/PC3 lab exhaust systems include:
Verification is a documented process showing compliance with design and correct implementation during construction and commissioning as well as assessing systems and equipment performance at specific limits and single point failure modes.
Critical system verification ensures the performance and compliance of systems such as building services, security, access control, emergency power biological safety cabinet systems, building management systems, waste and facility decontamination systems and emergency systems.
Verification documentation includes various documents like installation records, operational testing results and compliance certificates like certificates of construction compliance and results of failure mode tests. Verification procedures can vary according to your facility type and importance levels. Examples of verification procedures for containment laboratories include the following:
The main goal is to assess and refine operations to ensure the best facility performance during the Defects Liability Period (DLP). It involves refining building services performance based on gathered and analysed operational data over the first six to 12 months of the facility’s life activities.
Post occupancy optimisation typically occurs in three phases:
Key optimisation areas include environmental controls, energy systems improvements and safety systems refinements.
The integration of enhanced commissioning, verification and post occupancy optimisation creates a robust framework for ensuring laboratory and cleanroom facilities excellence. These processes, although complex and resource-intensive, are essential investments. Success in maintaining high-performance laboratories and cleanrooms requires a continuous commitment to these processes.
The long-term benefits of implementing these comprehensive processes include improved facility safety and reliability, enhanced operational efficiency, reduced maintenance costs, extended equipment lifespan, consistent regulatory compliance, better resource use and increased user satisfaction and productivity.
As laboratory and cleanroom facilities continue to evolve and advance, the importance of these processes will only grow. They are indispensable components in the management and operation of modern laboratories and cleanrooms.