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!