Maintaining and improving GMP compliance of cleanroom manufacturing operations is a mandatory requirement for all pharmaceutical manufacturers. In addition, cost and sustainability of manufacturing operations are an increasing focus, especially given the high energy consumption in most cleanrooms. In this talk, it will be shown how quality, efficiency and costs are related and how most manufacturing cleanrooms can be improved so that they deliver high quality environments, safely and efficiently, with significant cost reduction. It will include case studies ,where pharmaceutical manufacturers have successfully improved their cleanroom operations in both sterile and non-sterile production.

Speaker

Keith Beattie has over 20 years experience in the pharmaceutical industry in engineering, operations and facilities/utilities management. Most recently, he joined EECO2 Limited, a specialist-engineering consultancy focused on supporting global pharmaceutical and biotech clients with identification and delivery of energy and water reduction opportunities. The company has global expertise in cleanroom, energy efficient design, operations and GMP Quality compliance and combines these aspects to help clients create new high quality and efficient manufacturing operations and modify existing facilities to reduce cost and improve quality. Keith was a key contributor to developing recently published ISO 14644-16 (energy efficiency in cleanrooms) and is a member of ISPE HVAC/Sustainability COP steering committee. He is a Chartered Engineer, Chartered Energy Manager, ESOS (Energy) Lead Assessor and member of The Institute of Directors.

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