ValGenesis Inc., a provider of enterprise validation lifecycle management systems (VLMS), has announced that a rapidly expanding CDMO serving a global market, has selected ValGenesis e-Logbook to digitize logbook management across its manufacturing sites.

The company uses advanced nitrogen purging capabilities and is a fill/finish CDMO specializing in sterile filling of vials, syringes, and cartridges for the biotech and pharmaceutical industries. They chose ValGenesis e-Logbook for its ability to digitize the entire process, incorporating business rules to enforce operating procedures to optimize productivity, ensure compliance, and mitigate risk.

ValGenesis e-Logbook is a next-generation electronic logbook application, purpose-built for the stringent demands of the regulated life sciences industry. Part 11 and Annex 11 compliant, it can scale to thousands of users across multiple global sites, even working offline for strictly controlled and secured facilities.

“Transitioning from paper to electronic logbooks is becoming imperative for organizations seeking to streamline operations and maintain compliance,” says Steve Reynolds, Chief Revenue Officer at ValGenesis. “Central to the effectiveness of any electronic logbook software application is the integration of robust business rules to establish clear expectations and ensure consistent outcomes. This is possible with ValGenesis e-Logbook, as our customer is now aware. We are excited about our journey ahead with this rapidly evolving innovator.”