Health & life sciences
From R&D laboratories to full-scale biomanufacturing, we define, design and deliver mission-critical facilities (cleanrooms, laboratories and manufacturing facilities) that meet the most stringent regulatory standards. Our integrated approach ensures your infrastructure supports both today's operations and tomorrow's innovations.Health & life sciences
From R&D laboratories to full-scale biomanufacturing, we define, design and deliver mission-critical facilities (cleanrooms, laboratories and manufacturing facilities) that meet the most stringent regulatory standards. Our integrated approach ensures your infrastructure supports both today's operations and tomorrow's innovations.
Delivering compliant, future-ready environments for groundbreaking therapies
The health and life sciences sector is driven by intensive research and development, delivering breakthrough treatments in areas like cell and gene therapies (CGT), personalised medicine, and advanced biologics. The sector's greatest challenge is maintaining absolute quality and meeting strict regulatory compliance (cGMP, GAMP, ISO standards) while keeping pace with rapid technological and scientific progress.
This creates demanding facility requirements: rigorous aseptic and containment control, specialised sterilisation protocols (HTM 01-01), and infrastructure that must be both scalable and adaptable.
Organisations need integrated digital systems for complete traceability, must operate under continuous regulatory oversight, and require the flexibility to accommodate emerging therapies and evolving processes.
Success depends on facilities that function as compliant, future-ready environments, capable of supporting current operations while enabling tomorrow's innovations.
Markets we serve
Equans Sci-Tech is a proven partner for the health and life sciences sector, delivering highly regulated, technically advanced environments that stand the test of time. Our expertise covers the complete project lifecycle, from initial concept and design through construction, validation, and ongoing lifecycle optimisation.
Medical devices
We define, design and deliver the precision-controlled environments required for the manufacture of Class I, II, and III medical devices.
Pharmaceutical and biopharmaceutical
We deliver validated, GMP-compliant environments engineered to support the full drug development lifecycle, from primary research to secondary manufacturing.
We integrate advanced digital systems, clean utilities, process automation, and sustainable environments to future-proof your operations. Combined with deep knowledge of UK and European regulatory frameworks, this approach minimises risk, ensures compliance, and accelerates time-to-market for life-changing therapies.
Choosing Equans Sci-Tech means gaining integrated certainty from day one, delivering secure investment, reduced risk, and guaranteed long-term operational integrity for your most critical assets.
Find the answers to your questions
We integrate regulatory compliance into the very beginning of the define phase, rather than treating it as a final inspection. We ensure that every MEP system, air filtration unit, and surface finish is documented and tested to meet the latest UK and European standards, giving you total technical certainty for your audits.
Yes. We specialise in creating scalable environments that bridge the gap between discovery and production. Our team understands the differing rigour required for laboratory research versus aseptic manufacturing, allowing us to design flexible infrastructure that can adapt as your product moves through its clinical lifecycle.
We design robust segregation strategies using advanced HVAC systems, pressure cascades, and airlock configurations. By integrating smart automation and digital monitoring, we provide the precise environmental controls necessary to prevent cross-contamination, even in high-complexity environments handling multiple therapies or batches.
We define, design and deliver environments across the entire cleanliness spectrum, from ISO 9 (Controlled Non-Classified) through to ISO 5 (Grade A). Whether you require a high-level aseptic suite for sterile manufacturing or a lower-grade cleanroom for primary packaging and assembly, we provide the exact level of filtration and pressure control required. Our expertise ensures your environment remains compliant with cGMP, ISO 14644, and GAMP standards regardless of its classification.
Yes, we have extensive experience in delivering high-containment environments, including BSL-rated laboratories. We focus on the critical integration of airtight envelopes, specialised filtration (HEPA), and secure waste-management systems to ensure that both your personnel and the external environment remain fully protected.
Discover more
In a sector where precision and compliance are non-negotiable, having the right partner is essential. Explore who we are to learn about our specialist heritage, discover the breadth of what we do, or see how our commissioning process guarantees that your facility is fully validated and ready for critical operations.
Let's define, design and deliver the future together
Let's define, design and deliver the future together
