12.14.22 -- How To Improve Manufacturing Process Monitoring

To ensure that a commercial biomanufacturing process is in a state of control, life science companies must create and successfully execute initiatives to meet continued process verification (CPV) and other monitoring guidelines. Learn how to navigate the major steps of implementing a global monitoring plan for continued process verification.

Monitoring programs are implemented in order to adhere to regulatory guidelines, enhance understanding, reduce variability, improve process consistency and predictability, and more. Companies must aggregate their data in an automated and scalable fashion before they can monitor it. Learn how cost-effective, global process monitoring programs can make this process easier.

A leading organization in small molecule therapies was facing a challenge in ensuring consistent CPV initiatives across their different manufacturing sites were maintaining uniform data analytics standards. A software solution, purpose-built for biopharmaceutical manufacturing, provided a strong foundation to streamline the validation of manufacturing analytics for CPV and reporting.

Following several mergers and acquisitions, a biopharmaceutical company had to manage an increasing amount of data from disparate online and offline sources. A solution allowed them to access data from various sources and to feed other systems with data quickly to support the company’s digital science and manufacturing informatics strategies.