Consulting
Process Development
Analytical Services
GMP Manufacturing
Facility Design & Process EngineeringPurpose-built for flexibility, scalability, and regulatory excellence. Our GMP facility provides a process-agnostic, sustainable environment to support clinical and commercial manufacturing.
GMP Manufacturing
Our Facility
A Flexible, Scalable, and Sustainable GMP Facility
Bringing a cell or gene therapy to market requires a GMP-compliant manufacturing environment that supports efficient scale-up, process adaptability, and long-term commercial viability. Without the right infrastructure, companies face regulatory hurdles, operational inefficiencies, and production constraints.
Our 65,000ft² (6,000m²) GMP facility is designed to be flexible, process-agnostic, and scalable, ensuring we can support autologous and allogeneic cell therapy, viral vector, and RNA-based manufacturing.
With four fully qualified and operational Grade C cleanrooms, cutting-edge process capabilities, and a range of GMP-compliant storage solutions, including ambient, refrigerated, and deep-freeze options, we provide a seamless transition from process development to GMP production.
Sustainability is embedded throughout our facility, reducing energy consumption and operational costs while maintaining the highest regulatory standards.
Facility Capabilities
GMP Cleanroom Suites
Four independent, Grade C cleanrooms designed for viral vector, autologous, and allogeneic cell therapy manufacturing.
Process-Agnostic Design
Supporting multiple CGT modalities, with adaptable layouts for changing production needs.
Expansion Space
12,000ft² (1,100m²) of reserved capacity to accommodate future GMP manufacturing, including 500–1000L viral vector processes, RNA therapeutics, and emerging technologies.
Integrated Fill-Finish Suite
Grade A isolators for aseptic vial and bag filling, ensuring final product sterility and compliance.
Comprehensive Quality Control (QC) Laboratories
In-house QC for physiochemical, molecular, and biological testing, supporting batch release and stability studies.
GMP Storage
Secure storage for raw materials, intermediates, and final products at refrigerated, ultralow temperature and cryostorage conditions.
Warehouse & Logistics Support
GMP-compliant material management, including controlled receipt, storage, and distribution.
Energy-Efficient & Sustainable Design
The facility features solar panels, 10 EV charging points, and fossil fuel-free heating and cooling via heat pumps and exhaust air recovery.
Why Partner with Us?
Experience Our Facility Firsthand
Discover how our state-of-the-art GMP facility can support your clinical and commercial manufacturing needs. Contact us for a tour and explore the possibilities.
