- A leading sterile fill-finish CDMO has adopted ValGenesis’ electronic logbook platform to modernize GMP record management across global facilities.
- The cloud-based solution supports thousands of users, enables real-time data capture, and replaces paper logbooks to improve compliance and scalability.
ValGenesis, Inc. has announced that a leading fill-finish contract development and manufacturing organization (CDMO) specializing in sterile filling has adopted its electronic logbook application to modernize logbook management across its manufacturing facilities.
The implementation replaces hundreds of paper logbooks that had become difficult to manage as the CDMO expanded operations to include advanced robotic manufacturing lines and increasingly sophisticated equipment. The new system enables real-time data capture, automated compliance checks, and seamless traceability across multiple global sites.
The cloud-based electronic logbook platform is designed to meet GMP requirements within the life sciences industry. It allows users to digitally capture, track, and maintain logbooks across multiple devices. The application supports thousands of users and includes offline functionality for secure, controlled environments to ensure continuous and compliant operations.
According to the company, the digital transition strengthens its quality management system and optimizes resource utilization. Data collected through the system adheres to ALCOA+ data integrity principles while supporting improved operational efficiency and accelerated timelines for clients.
“We’re excited to support this customer in their digital transformation journey. By replacing paper-based logbooks with ValGenesis, the company is strengthening compliance, improving operational efficiency, and ensuring scalability as it continues to grow and adopt advanced manufacturing technologies.”
Steve Reynolds, Chief Revenue Officer at ValGenesis
