O’Neal’s core capabilities in clean space design, process
engineering, critical utilities, and cGMP equipment engineering provide the
necessary foundation for the successful execution of pharmaceutical facility
design projects—from concept through detailed design.

cGMP Pharmaceutical Facility Design

Pharmaceutical manufacturing requires an environment designed to meet cGMP standards—to ensure the safety, identity, strength, quality, and purity of the product. Quality assurance and contamination control are key requirements, and O’Neal brings the skill-set and engineering experience to ensure that your process, utilities and manufacturing space is designed to meet the rigorous demands of an FDA-licensed facility. This is an absolute requirement for facilities that are designed for drug substance (API) and drug product (fill/finish) manufacturing.

Engineering Capabilities

O’Neal has extensive pharmaceutical facility design experience includes those for research, process development, clinical manufacturing, and cGMP production. Regardless of whether your goal is to expand API manufacturing or to build a pharmaceutical fill/finish and packaging plant, O’Neal can provide the appropriate design solutions to meet your business need.

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