Tag: GMP

Navigating the Path of Annex 1 Compliance: A Journey towards Regulatory Adherence and Batch Release

Presented by: Connie Leech, Global Director Quality, Compliance & Regulatory Affairs , CAI Top Reasons to watch Comprehensive Overview: Get a comprehensive overview of Annex 1 and its role in ensuring the sterility and quality of medicinal products, empowering you with essential knowledge for your role in the industry. Expert Insights: Gain valuable insights from […]

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Establishing CAPA to Support Your Investigation And Promote Continuous Improvement

Presented By: LeAnna Pearson, Associate Director Quality Compliance & Regulatory, CAI Part 1 – CAPA 101 back to basics• Understand the purpose and history behind the CAPA• Understand what the FDA is expecting from your CAPA• Understand when to use a CAPA• Review the typical CAPA processPart 2 – Building blocks of an effective CAPA […]

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Removing Bias from Quality Risk Management in Pharma and Biopharma Operations

Presented By:Pedro Ferreira, Quality Risk Management Tech Lead, ValGenesis Margarida Ventura, Quality Risk Management Consulting Lead, ValGenesis Dr. Iris Ziegler, Director Pharmaceutical Sciences and QbD, Corden Pharma International Part 1 – Commercial and Lifecycle Implementations of Quality Risk Management• Draw a baseline on what QRM is in terms of goals and context• Understand the QRM […]

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A Sustainable Model For Production System Excellence

Presented By: Woon Lit Ong, Senior Director, APAC & AfME Operational Excellence, Pfizer Global Supply and Rajnish Narula, Director, Business Excellence, Tuas, Pfizer Global Supply Learn about the design, deployment and sustainment of the Pfizer Production System called Integrated Manufacturing Excellence (IMEx, similar to the Toyota Production System TPS). IMEX helps to establish a standardized […]

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