Facility Design & Process Engineering

Concept Design

Laying the foundation for scalable, GMP-compliant facilities. Our Concept Design services ensure process efficiency, regulatory readiness, and seamless facility development for cell and gene therapy manufacturing.

Building a Strong Foundation for CGT Manufacturing

Successful Cell and Gene therapy (CGT) manufacturing starts with a well-planned facility fitting around a well-defined set of process(es). Without strategic early-stage design, companies risk regulatory hurdles, inefficient workflows, and costly retrofits. Our approach ensures that every aspect of facility design—from process integration to regulatory compliance—is strategically planned from the outset, reducing long-term risk and accelerating time to market.

We provide tailored facility solutions, ensuring your manufacturing space and support spaces are GMP-ready, process-efficient, and scalable for future growth. Our expertise covers a broad range of CGT modalities, including autologous and allogeneic cell therapies, viral vectors, and RNA-based therapeutics.

Our Approach

Our Concept Design services transform facility requirements into practical, efficient layouts that support long-term success.

We take a comprehensive, solutions-driven approach to facility planning, ensuring that cleanroom configurations and HVAC options, process flows, and compliance frameworks are seamlessly integrated from the outset. By considering personnel movement, material flow, and equipment positioning, we create GMP-compliant spaces that optimise both operational efficiency and long-term scalability. Through early-stage visualisation and collaborative design reviews, we help clients refine their facility concepts to align with regulatory expectations and future production needs.

Key deliverables

Process Flow Mapping

Defining how materials, personnel, and equipment interact to ensure operational efficiency.

Facility Layout Development

Creating GMP-compliant, process-optimised cleanroom designs.

Personnel, Material and Waste Flows

GMP compliant optimised flows and adjacencies

HVAC Zones and Pressures

Providing suitable containment for product and operator protection, HVAC Rationals backed up by suitable HVAC configurations

3d Designs and Equipment models

Utilising our extensive 3d Cell and Gene Therapy model database we can quickly visualise and optimise room sizes.

Equipment & Technology Integration

Ensuring seamless alignment with process and operational needs.

GMP User Requirements Specifications

Produced for piecemeal built systems on a design and build basis

Regulatory & Compliance Planning

Embedding global GMP, MHRA, FDA, and EMA requirements into facility design.

Scalability Considerations

Designing adaptable facilities to support future process changes and capacity expansion.

Why Partner with Us?

Industry Experts

Decades of experience in CGT facility planning and process engineering.

Regulatory Foresight

Integrating compliance from the earliest design stages.

Support

Seamless transition from Concept Design to facility construction and GMP operations.

Customised Solutions

Process-agnostic designs tailored to cell therapy, viral vector, and RNA manufacturing.

Plan for Success with eXmoor Pharma

The right facility design ensures regulatory compliance, operational efficiency, and long-term scalability. Let’s build a foundation for your success. Contact us to discuss your facility concept design needs.

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Our Process Engineering Services

Process Engineering

Optimising facility and process design for seamless, cost-effective, and GMP-compliant Cell and Gene Therapy manufacturing.