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This presentation will delve into the concept of a modular approach to pharma quality management, breaking it down into smaller, more manageable components such as Business Process Management, Documents & Records Management, GRC, and Regulatory Management. By examining each component in detail, we will understand how their integration can revolutionize quality management practices within the pharmaceutical industry. We will highlight the advantages of adopting this modular approach, such as improved efficiency, enhanced process control with fully automated processes, and reduced costs. Additionally, we will delve into the transformative potential of data analytics and data visualization in identifying trends, risks, and areas for improvement within the quality management system.