AiX provides end-to-end engineering solutions for medical device manufacturing facilities, ensuring compliance with global standards such as ISO 13485, USFDA, and CE. Our services cover facility planning, cleanroom design, utilities, and validation support, delivering efficient, compliant and future-ready infrastructure.
Read MoreWith the clear understanding of all kinds of Dosage process and in-depth knowledge of regulatory requirements, cGMP standards, local regulatory standards, Air classification, cleanliness and other major engineering insights, we design state-of-the-art pharmaceutical dosage form facilities.
Read MoreAt AiX, we leverage our extensive knowledge & experience in the design and execution of biopharmaceutical facilities. Our capabilities encompass a wide array of crucial elements, including process design, batch sizing calculations, risk analysis (FMEA) associated.
Read MoreWith a comprehensive understanding of various extraction, filtration, separation processes, dosage processes and a deep knowledge of regulatory requirements, cGMP (Current Good Manufacturing Practices) standards, local regulations and other critical engineering aspects.
Read MoreOur team, with wide and comprehensive experience, we specialize in the design of laboratories that encompass a comprehensive range of elements, ensuring that these spaces meet the highest standards for functionality, safety and sustainability.
Read MoreWe conduct precise throughput-based calculations to define storage conditions & automation levels. Our expertise includes analyzing turnaround times & optimizing loading/unloading strategies. We specialize in efficient space planning tailored to operational demands.
Read MoreWith vast experience in the industrial project sector, our team delivers reliable, innovative engineering solutions. We specialize in addressing complex industrial challenges with tailored approaches. We ensure each project is delivered with precision, efficiency, and long-term value.
Read MoreWith specialized expertise in the pharmaceutical sector, the team excels in the design, engineering and execution of API and Bulk Drug manufacturing facilities. Built on a solid foundation of regulatory compliance and advanced process engineering, the focus is on delivering turnkey solutions.
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