Customer Stories and Testimonials

"Veeva has a broad range of applications that fit what Alcon needed as a medical devices company. One platform, unified, in the cloud, multi-tenant that truly match what Alcon was looking for in the software."

"Partnering with Veeva MedTech supports us in our strategy of utilizing new technologies and improving internal processes and structures with the help of digital excellence."

"There are many good vendors out there, but Veeva MedTech impressed us the most in their platform. Their thirst to hear what customer needs are, and adapt to make changes, periodic updates on an annual basis, several times a year, were also a plus."

"Shifting away from paper-based and manual processes gives us valuable time back and allows our clinical operations team to focus on driving trial results and innovation."

"We needed a scalable, global, and easy-to-search document management solution that would adapt to our expanding business needs and meet multiple stakeholder requirements. Veeva Vault is transforming how our employees access and manage critical documentation.”

"The Veeva platform has allowed us to be always audit-ready. So if a regulatory agency comes in we are prepared to undergo an audit on their schedule."

"Partnering with Veeva MedTech enabled us to harmonize our global quality assurance and regulatory affairs processes with a single source of content and data. With complete visibility throughout our change management processes, we can make more informed decisions and get products to market much faster."

"We are modernizing our trial processes with Vault Clinical Suite to streamline studies from build to close, accelerating the development of potential life-changing cancer tests."

"Veeva MedTech delivers a platform that will scale as we develop new products and expand into global markets. Being able to run trials end-to-end on a connected system provides the visibility and control to speed our total product lifecycle."

"With thousands of products in over 130 countries, it historically took hundreds of hours to report. With Vault RIM, a single report instantly generates all approvals and renewals, saving us approximately 200 hours per year."

"Vault eTMF allows us to manage study documents more efficiently and with a high level of quality. We now have a system that provides precision and speed to support our evidence needs."

"Veeva Vault allows us to quickly adapt to changing compliance and business requirements by providing tighter control over data and documents and real-time visibility across teams. We’ve been able to unify key business processes with Veeva MedTech so we’re more agile, easily pivoting direction to prevent delays."

"Our mission is to streamline and minimize error during cancer diagnosis and adopting best-in-class technology is key to reaching our goals. By leveraging Veeva Vault QMS and Veeva Vault QualityDocs, we are well-equipped to move our products into the next stage of development while remaining compliant with current industry regulations."

"We needed the flexibility to build studies how we want and get them up and running fast. Veeva MedTech helps us streamline processes with greater control, improving compliance across clinical data and operations."

“Using Vault QualityDocs as our comprehensive solution for GMP activities has increased our data integrity and document control to remain compliant. The cloud-based, collaborative functionality allows us to be more agile.”

“Having all content in a single, globally accessible platform with an automated workflow has allowed us to create, approve, and distribute content to accelerate our time-to-market speeds in a way that was not possible before.”

"Veeva MedTech allowed us to streamline quality across all of our manufacturing sites to get ventilators to the patients that need them faster. The speed of the Veeva team was critical to helping us produce such a large volume of devices in under three months."