GMP-compliant facilities for pharma, biotech & medical devices across MENA.
About Us
At Agon Engineering, we don’t just build pharmaceutical and biotech facilities—we engineer them to meet regulatory scrutiny from the ground up. Every design, every duct, every layout is built to withstand the toughest inspections, whether by WHO, EMA, SFDA, or US FDA.
From concept to commissioning, Agon Engineering delivers future-ready, compliant, and scalable solutions.
We design, build, and validate pharma facilities that meet global standards—delivering compliance, efficiency, and scalability from cleanrooms to turnkey execution.
Agon Engineering provides end-to-end pharmaceutical engineering services, including GMP-compliant facility layout design, turnkey execution, CQV (Commissioning, Qualification, and Validation) services, HVAC & BMS utility planning, and comprehensive documentation services like VMP, URS, FDS, and Risk Assessments.
Our expertise in pharmaceutical infrastructure combines precision-driven engineering with a deep understanding of industry standards. We provide modular, GMP-compliant solutions and have a proven track record in designing and executing complex projects in the pharma and biopharma sectors.
We serve a wide range of pharmaceutical sectors, including:
GMP-compliant facility design involves creating spaces that adhere to Good Manufacturing Practice (GMP) standards. This includes proper HVAC zoning, contamination control, and ensuring compliance with regulatory requirements to safeguard product quality.
Our turnkey execution services cover the entire lifecycle of cleanroom and pharma facility construction. From modular cleanroom builds to MEP (Mechanical, Electrical, and Plumbing) execution, we handle everything from design to final delivery.
CQV stands for Commissioning, Qualification, and Validation. It is essential to ensure that all equipment, systems, and facilities function according to the required specifications and are compliant with industry regulations. Our services include DQ, IQ, OQ, and PQ protocols to verify the systems' effectiveness.
