Pharmaceuticals

Pharmaceutical Engineering Experience

DME Alliance has design experience with a variety of pharma facilities including those for research, process development, clinical manufacturing and cGMP production. Company engineering, process science, and regulatory compliance capabilities are uniquely suited to deliver solutions for operations that manufacture parenteral, solid dosage, bulk chemical, potent compound and compounding pharmacy products. Over 90% of engineering and design services are delivered to the regulated life sciences industry.

Facility Design for GMP Compliance

Pharmaceutical manufacturing requires an environment that is designed to meet cGMP standards to ensure the safety, identity, strength, quality, and purity of the product. Product quality assurance and contamination control are key requirements, and DME Alliance 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 a key requirement for facilities that are designed for drug substance (API) and drug product (fill/finish) manufacturing.

Engineering Capabilities

Core capabilities in clean space design, process engineering, critical utilities and GMP equipment engineering provide a foundation for the successful execution of pharmaceutical projects from concept through detailed design. Regardless of whether your goal is to expand clinical manufacturing or to build a GMP production plant, DME Alliance can provide the appropriate design solutions to meet your business need.

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