Integrating design precision, turnkey excellence, and sustainable modular innovation to build a healthier tomorrow

The pharmaceutical facility landscape is clearly complex today.

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The industry challenge and a holistic solution

In your view, what is the single biggest pitfall companies face when starting a major construction or expansion project?

The biggest pitfall is a lack of upfront integration. Building a modern facility isn't just construction; it must seamlessly integrate process design, utilities, automation, and rigorous regulatory compliance (like USFDA guidelines, cGMP, and Annex 1, etc.) all at once. Many issues arise simply because integration is considered late in the process, rather than from the very start, leading to fragmented execution and costly rework.

How does Pharma Access fundamentally change the traditional approach to designing and building these facilities?

We've pioneered a holistic approach we call 'Integration from the Ground Up.' We embed compliance and efficiency from the outset. By baking regulatory considerations into every phase, from conceptualization to commissioning we ensure the final facility is not only compliant but also optimized for seamless, high-performance operation.

Predictive design and quality assurance

Your team relies heavily on 'Simulation-Based Engineering.' What is the practical benefit of building a digital twin before laying the first brick?

Simulation is a powerful predictive tool. saving time, money, and compliance headaches. We build virtual replicas, a complete digital twin of process flows, HVAC systems, piping, and electrical circuits. This allows us to anticipate operational challenges and optimize system layouts virtually, drastically reducing the risk of costly field modifications. For example, we use Computational Fluid Dynamics (CFD) simulations for cleanroom design to guarantee adherence to ISO 14644 standards, calculating the precise Air Changes Per Hour (ACH):

ACH = Q x 60/V