Case Study: AstraZeneca achieves unified digital validation and faster manufacturing growth with Veeva Quality Cloud

AstraZeneca prepares 32-site manufacturing growth with Veeva Validation Management

AstraZeneca, a large biopharma, faced compliance risks and inefficiency due to paper-based and site-specific validation processes across its global manufacturing network. This challenge hindered visibility and created duplicative work as the company prepared for ambitious growth. To achieve a unified digital validation system, AstraZeneca partnered with Veeva Systems, implementing Veeva Quality Cloud solutions including Veeva QMS, Veeva QualityDocs, and Veeva Validation Management.

The solution from Veeva created a single source of truth, integrating quality and validation processes into one platform. This eliminated paper binders, improved data integrity, and increased compliance. AstraZeneca now benefits from continuous innovation through Veeva's updates and expects future efficiency gains through risk-based validation and AI. The shift supports the company's manufacturing growth goals with a streamlined, electronic system.

AstraZeneca