Isolator & Containment Technical Support
Our dedicated Isolator and Containment Subject Matter Experts (SMEs) provide specialist technical support for pharmaceutical manufacturing projects across global client programmes.
We deliver end to end expertise to support the successful design, integration, commissioning, and validation of isolator systems, ensuring compliance with GMP, Annex 1, and industry best practices.
Isolators sit at the heart of sterile and high containment manufacturing, and the decisions made at each stage of a project have a lasting impact on product quality, operator safety and regulatory outcomes. Our SMEs bring hands on experience across a wide range of isolator technologies, from aseptic filling and sterility testing systems through to high potency containment applications.
This practical background means we understand not only how systems should be specified on paper, but how they behave in operation and where projects typically encounter problems. Working collaboratively with manufacturers, engineering teams, and end users, we help deliver compliant, efficient, and robust isolator solutions for sterile and high containment pharmaceutical environments.
Our support includes
Isolator system design reviews and technical consultancy
P&ID, layout, and process integration support
Containment strategy and aseptic processing guidance
Risk assessments including HAZOP and contamination control reviews
Factory Acceptance Testing (FAT) and Site Acceptance Testing (SAT)
Commissioning, Qualification, and Validation support (IQ/OQ/PQ)
Operational optimisation for safe, reliable, and high performance systems
