Manufacturing Bottlenecks: Why Analog Cleaning Validation Programs Slow Down Your Entire Operation

Kenneth Pierce (Director of Product, Process & Cleaning Validation Lifecycle) will present the webinar Manufacturing Bottlenecks: Why Analog Cleaning Validation Programs Slow Down Your Entire Operation on May 14, at 8:00 AM EDT. There is a second session at 12:00 PM EDT.

Cleaning validation programs are complex to plan and deliver due to the multitude of regulatory, patient safety, and product quality requirements. Keeping control of their delivery in an analog mode—primarily on paper—has always been a challenge due to the number of protocols, sampling operations, people, and potential points of failure involved.  

Continuing to manage cleaning validation and ongoing verification via paper-based processes is slowing down your entire manufacturing operation and limiting the number of batches you can release each year. Transitioning to a digitalized process on a robust, validated SaaS platform can improve consistency of approach through frameworks and workflows, and drive efficiency through centralized data management and approval processes. Empower your operations team with higher overall equipment effectiveness (OEE) and reduced deviations—digitalize today!   

Even if you are not able to attend the live event, we still recommend registering in order to receive a link to the full recording.

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