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In order to comply with widely established GMP regulations requiring "minimizing the risk of contamination caused by recirculation or re-entry of untreated or insufficiently treated air…" An evaluation of potential for cross-contamination via HVAC should be part of the risk assessment in multi-product facilities.
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Norman A. Goldschmidt
PRINCIPAL, ENGINEERING
Is a Sustainable cGMP Manufacturing Facility Achievable? In 1999, 16% of the world's population consumed 80% of its natural resources. The United States, with 4% of the world's population, consumed 25% of the world's natural resources.
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Bernard C. Friel, PE
ENGINEERING, PRESIDENT & PRINCIPAL
GSK US Biopharms, Global Manufacturing & Supply, Primary Supply & Antibiotics. Most pharmaceutical sites have a requirement for process chillers or for process refrigeration systems.
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Contributor: Derek Demchak
PROJECT ENGINEER, MECHANICAL
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Our subject matter experts speak at conferences and share their knowledge in areas such as Energy and Sustainability, cGMP Compliance, and Central Utilities through whitepapers.
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