DME’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 DME 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.
DME 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, DME can provide the appropriate design solutions to meet your business need.