Veeva Quality Cloud Enhances Kindeva's Manufacturing Operations and Efficiency
In a significant leap towards modernizing its manufacturing operations, Kindeva has announced the adoption of Veeva Quality Cloud. This transition aims to unify Kindeva's global network of sites onto a single cloud-based quality platform. Veeva's suite, which includes QualityDocs, QMS, Training, and LearnGxP, equips Kindeva with a scalable technological foundation designed to meet emerging customer demands as the company continues its growth trajectory.
Melanie Cerullo, Kindeva’s Quality Director, emphasized the company's commitment to developing therapies that can significantly improve patient outcomes. "By implementing Veeva Quality Cloud, we will enhance our quality management infrastructure, supporting greater standardization, real-time visibility of operations, effective collaboration, and secure information exchange with our clients. This ensures compliance with global regulations and enables Kindeva to produce high-quality products at scale while driving operational efficiency throughout the value chain," she stated.
The integration of Veeva Quality Cloud will standardize and unify Kindeva's business processes. By linking quality assurance (QA) and training, this contract development and manufacturing organization (CDMO) will operate more efficiently and eradicate data silos. The platform empowers Kindeva to deliver superior service to its clients and expand into new regions and therapeutic areas, particularly as it advances its filling and finishing operations.
"Veeva is a key partner in realizing our vision of digital quality, helping us streamline our system infrastructure across the organization while ensuring data integrity," remarked Prakash Pandian, Kindeva's Chief Information Officer. He added that "with Veeva Quality Cloud, we can establish standardized global procedures that enhance site productivity and create added value for our enterprise, our clients, and ultimately our patients."
Veeva Quality Cloud's capabilities to unify quality processes, integrate applications, and promote collaboration are crucial in reducing cycle times and maximizing efficiency. For more information about Veeva Quality Cloud tailored for CDMOs, visit veeva.com/eu/Quality-CDMO.
About Veeva Systems
Veeva offers a cloud-based platform for the life sciences industry, providing software, AI, data, and consulting services. Committed to innovation, product excellence, and client success, Veeva serves over 1,500 customers, including the largest global biopharmaceutical firms and emerging biotechnology companies. As a public benefit corporation, Veeva aims to balance the interests of all stakeholders, including customers, employees, shareholders, and the industries it serves. Learn more at veeva.com/eu.
Statements Regarding Forward-Looking Information
This announcement contains forward-looking statements concerning Veeva’s products and services and the anticipated results or benefits from using our offerings. These statements are based on current expectations, and actual outcomes may differ significantly. Various risks could adversely affect our outcomes, including those disclosed in our 10-K filing for the fiscal year ending January 31, 2026, which can be reviewed at the SEC’s site. Risk summaries are available on pages 13 and 14 of the filing and in subsequent SEC documents.
Melanie Cerullo, Kindeva’s Quality Director, emphasized the company's commitment to developing therapies that can significantly improve patient outcomes. "By implementing Veeva Quality Cloud, we will enhance our quality management infrastructure, supporting greater standardization, real-time visibility of operations, effective collaboration, and secure information exchange with our clients. This ensures compliance with global regulations and enables Kindeva to produce high-quality products at scale while driving operational efficiency throughout the value chain," she stated.
The integration of Veeva Quality Cloud will standardize and unify Kindeva's business processes. By linking quality assurance (QA) and training, this contract development and manufacturing organization (CDMO) will operate more efficiently and eradicate data silos. The platform empowers Kindeva to deliver superior service to its clients and expand into new regions and therapeutic areas, particularly as it advances its filling and finishing operations.
"Veeva is a key partner in realizing our vision of digital quality, helping us streamline our system infrastructure across the organization while ensuring data integrity," remarked Prakash Pandian, Kindeva's Chief Information Officer. He added that "with Veeva Quality Cloud, we can establish standardized global procedures that enhance site productivity and create added value for our enterprise, our clients, and ultimately our patients."
Veeva Quality Cloud's capabilities to unify quality processes, integrate applications, and promote collaboration are crucial in reducing cycle times and maximizing efficiency. For more information about Veeva Quality Cloud tailored for CDMOs, visit veeva.com/eu/Quality-CDMO.
About Veeva Systems
Veeva offers a cloud-based platform for the life sciences industry, providing software, AI, data, and consulting services. Committed to innovation, product excellence, and client success, Veeva serves over 1,500 customers, including the largest global biopharmaceutical firms and emerging biotechnology companies. As a public benefit corporation, Veeva aims to balance the interests of all stakeholders, including customers, employees, shareholders, and the industries it serves. Learn more at veeva.com/eu.
Statements Regarding Forward-Looking Information
This announcement contains forward-looking statements concerning Veeva’s products and services and the anticipated results or benefits from using our offerings. These statements are based on current expectations, and actual outcomes may differ significantly. Various risks could adversely affect our outcomes, including those disclosed in our 10-K filing for the fiscal year ending January 31, 2026, which can be reviewed at the SEC’s site. Risk summaries are available on pages 13 and 14 of the filing and in subsequent SEC documents.
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