The validation process in MES (Manufacturing Execution Systems) for pharmaceutical manufacturing often poses significant challenges due to the complex interplay between global standards and local site-specific requirements. This session will delve into the development and implementation of a global MES validation model that reduced validation errors by 60%. The approach integrates standardized functionalities, global risk assessments, and local connectivity to achieve seamless integration with site-specific equipment. Explore how leveraging a core system with proven global configurations minimizes redundancy, optimizes processes, and ensures regulatory compliance. In this session, you will learn how to:
- Implement a global MES validation model to reduce errors and streamline processes.
- Optimize validation by leveraging standardized configurations and global risk assessments.
- Ensure seamless local connectivity with site-specific equipment while maintaining global consistency.
- Minimize repetitive testing efforts through proven global functionalities.
- Balance global standardization with independent site-by-site adaptability for effective operations.
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