How to Optimise Your EM Programme
Incubation, Automation, and the True Cost of Quality in Pharma QC
This webinar, featuring expert insights from Genevieve Greene and James Flynn, from NIBRT, and Florian Morillon, from bioMérieux, explores the evolving landscape of Environmental Monitoring (EM) and quality practices within the pharmaceutical industry. It delves into topics including:
- Transitioning from dual to single temperature incubation in EM
- Strategic media selection for microbial recovery
- Preparing for audits: manual vs automated EM, system governance, and data integrity
- Leveraging electronic systems to enhance compliance and efficiency
- Evaluating the cost of quality and its broader impact across pharmaceutical operations
Watch the webinar replay to learn practical perspectives on how to optimize your EM workflows and strengthen audit readiness.
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