Designing a technically complex facility for drug product manufacturing requires both cGMP design expertise and the ability to mitigate risk through facility programming, layout, and technology selection. O’Neal’s engineers, designers and subject matter experts leverage these capabilities to provide innovative, flexible design solutions for both new facilities and legacy upgrades or renovations.

Risk management is job #1. We understand the issues associated with quality risk management and product contamination prevention in a cGMP fill/finish facility. Risk-based design is so engrained in our culture; it touches every aspect of our project delivery.

But we also deliver pragmatic, cost-effective solutions. At the end of the day, what matters most is that your facility is able to manufacture a high quality product with the capacity, flexibility, and cost of goods that meet your business requirements. O’Neal works with you to design and deliver formulation and filling capabilities—at the appropriate scale to fit your needs and budget.

Aseptic manufacturing? No problem! O’Neal has unique technical capabilities designing sterile manufacturing facilities. Our experience and expertise in compounding, lyophilization, RABS & isolators for aseptic processing, single-use (disposables) technology, and biohazard and potent compound containment are second to none.  Contact O’Neal to deliver fill finish facility design for high quality and cost-effective solutions.