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Pharmaceutical engineering focuses on designing, building, and optimizing manufacturing facilities of medicinal products.
One of the most important distinctions between pharmaceutical engineering and other engineering sectors is the pharmaceutical industry’s strict requirements for good manufacturing practice (GMP). For the outstanding performance of your pharmaceutical company, you must be able to handle increasingly complex GMP demands to ensure the medicine produced is safe for patients. GMP considerations are vital in all design phases, from early conceptual design to the implementation and execution of a pharmaceutical quality system.
Unlike other engineering consultant companies, our multidisciplinary team of pharmaceutical facility design architects and engineers and cleanroom validation, testing and processing engineers is expert in the complex and highly-regulated pharmaceutical industry. Whether you need a new facility or want to revamp an existing one, our goal is to help you achieve optimal GMP manufacturing using Lean principles and bring medical products quickly and safely to market while finding innovative ways to lower costs, increase output and improve sustainability.
Conceptual Design, Front-End Engineering Design (FEED) study, Detail Design, Procurement and Construction (EPC) in a Turn-key model, are some examples of added value we can generate with you.
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