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The Contamination Control Program: Engineering equips Engineering personnel with essential knowledge in facility design, contamination risk mitigation, sterilization, and regulatory compliance, ensuring GMP-compliant manufacturing environments. Program Modules: Risk Minimisation – Design, Cleanrooms, Validation – Best practices in facility layout, HVAC, and cleanroom validation. Measures to Mitigate Contamination Risks – Engineering controls for contamination prevention in equipment, utilities, and materials. Fundamentals of Cleaning & Sterilisation – Principles of cleaning validation, sterilization methods, and their applications. Understanding Contamination Risks – Key risks related to HVAC, airflows, utilities, and personnel movement. EU Annex 1 (Parts 1-3) – Regulatory expectations for sterile manufacturing, cleanroom operations, and contamination control strategy. Closed vs Open Processing – Engineering considerations for system design and sterility assurance. EU ATMP Guidelines (Parts 1 & 2) – Compliance requirements for Advanced Therapy Medicinal Products (ATMPs). Barrier Technology & Single Use Systems – Implementation of Isolators, RABS, and disposable technologies. Future Trends & Advancements – Emerging technologies, automation, and regulatory developments. This program ensures engineering teams can design, maintain, and optimize contamination-free manufacturing environments while ensuring regulatory compliance. For expert guidance, contact Pharmalliance Consulting Ltd at www.pharmalliance.ie.