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The Contamination Control Program: Manufacturing provides Manufacturing personnel with essential training on contamination prevention, cleaning, sterilization, and facility design, ensuring compliance with GMP, Annex 1, and ATMP guidelines. Program Modules: Relevance to Non-Sterile, Sterile, and ATMP Products – Contamination control strategies tailored to different product types. Risk Minimisation – Design, Cleanrooms, Validation – Best practices in facility design, cleanroom operation, and validation to prevent contamination. Measures to Mitigate Contamination Risks – Effective strategies for contamination control in materials, equipment, and personnel practices. Fundamentals of Cleaning – Essential cleaning protocols to maintain GMP-compliant environments and minimize microbial risk. Cleaning Agent Selection and Sampling – Proper selection and validation of cleaning agents for effective microbial and particulate removal. Fundamentals and Types of Sterilisation – Overview of steam, dry heat, gas, and radiation sterilization and their applications in pharmaceutical manufacturing. Disinfectants – Selection, validation, and regulatory expectations for disinfectant use in cleanroom environments. Understanding Contamination Risks Associated with Facilities and Cleanrooms – Identifying and mitigating risks related to HVAC, airflows, personnel movement, and material transfer. Closed vs Open Processing – Comparison of closed vs. open systems and their impact on contamination control and sterility assurance. This program ensures manufacturing personnel are equipped with the knowledge and skills to maintain contamination-free production environments, reducing risks and enhancing compliance. For expert guidance, contact Pharmalliance Consulting Ltd at www.pharmalliance.ie.