BioDlink announced the successful go-live of Veeva QMS, marking a key milestone in the company's quality digitalization strategy. The system officially entered operation following a launch event held on January 29 with representatives from Veeva and the joint project team. By implementing Veeva QMS, a globally recognized platform adopted across the life sciences industry, BioDlink aims to enhance the efficiency, accuracy, and compliance of its GMP-compliant manufacturing and quality processes, supporting global partners in the development and commercialization of innovative therapies.

The initial deployment covers four core quality processes: Deviation Management, Change Management, Laboratory investigation, and Corrective and Preventive Action (CAPA) Management. This implementation establishes a digital, standardized, and end-to-end quality operations framework. Additional modules, including Quality Risk Management, Audit Management, Supplier Management, Annual Product Quality Review, and Management Review, are planned for future phases to further strengthen the company's quality system.

Veeva QMS is a cloud-based quality management system purpose-built for the life sciences industry, designed to help organizations address complex regulatory requirements and the growing demands of modern quality management. Today, more than 300 companies worldwide streamline quality processes with Veeva QMS, including 17 of the Top 20 global pharmas. The implementation further strengthens BioDlink's quality and compliance capabilities while delivering a transparent, end-to-end digital quality platform to support global biopharmaceutical partners and accelerate the delivery of innovative therapies worldwide.