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AmplifyBio to Drive Quality Excellence with ³Ô¹Ï±¬ÁÏ Vault Quality Suite

Fast-growing CRO will bring together quality processes, content, and training to
streamline quality management and accelerate preclinical validation for cutting-edge medicines

PLEASANTON, CA ¡ª May 3, 2022 - ³Ô¹Ï±¬ÁÏ Systems (NYSE: VEEV) today announced that AmplifyBio is building a foundation for advanced quality, study execution, and reporting with ³Ô¹Ï±¬ÁÏ Vault Quality Suite. Using a modern quality system with built-in industry best practices, the company will streamline and automate processes to increase the efficiency of its preclinical drug testing.

¡°At AmplifyBio, we generate and report critical data through short and long duration studies that go into FDA submissions for many of our clients at a key stage in developing medicines,¡± said Jerry Hacker, executive vice president and chief commercial officer at AmplifyBio. ¡°With our state-of-the-art facility and ³Ô¹Ï±¬ÁÏ Vault Quality Suite, we will deliver data our clients can rely on while keeping up with the most rigorous GLP requirements.¡±

AmplifyBio is a contract research organization (CRO) focused on toxicology, safety pharmacology, and efficacy testing to accelerate innovation across pharmaceutical modalities. The company will use ³Ô¹Ï±¬ÁÏ Vault QMS to execute core quality processes, ³Ô¹Ï±¬ÁÏ Vault QualityDocs to manage and share SOPs and other GLP documents, and ³Ô¹Ï±¬ÁÏ Vault Training to ensure role-based qualifications. By managing end-to-end quality in a single system, AmplifyBio will be able to ensure quality excellence across its departments and suppliers.

¡°As a trusted partner, we¡¯re proud to support AmplifyBio¡¯s vision of advancing medical breakthroughs and cures for disease,¡± said Ashley Wentworth, senior director, ³Ô¹Ï±¬ÁÏ Vault Quality strategy. ¡°With ³Ô¹Ï±¬ÁÏ Vault Quality Suite, AmplifyBio will have a technology foundation that can scale and keep up with evolving customer and market needs.¡±

Vault Quality Suite includes Vault QMS, ³Ô¹Ï±¬ÁÏ Vault Product Surveillance, Vault QualityDocs, ³Ô¹Ï±¬ÁÏ Vault Validation Management, ³Ô¹Ï±¬ÁÏ Vault Station Manager, Vault Training, , and ³Ô¹Ï±¬ÁÏ Vault LIMS to automate and harmonize quality processes globally. Vault Quality Suite enables companies to easily manage quality in one unified solution and delivers the power and scalability needed across the life sciences value chain.

Additional Information
For more on ³Ô¹Ï±¬ÁÏ Vault Quality Suite, visit: veeva.com/VaultQuality
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About ³Ô¹Ï±¬ÁÏ Systems
³Ô¹Ï±¬ÁÏ is the global leader in cloud software for the life sciences industry. Committed to innovation, product excellence, and customer success, ³Ô¹Ï±¬ÁÏ serves more than 1,000 customers, ranging from the world¡¯s largest pharmaceutical companies to emerging biotechs. As a Public Benefit Corporation, ³Ô¹Ï±¬ÁÏ is committed to balancing the interests of all stakeholders, including customers, employees, shareholders, and the industries it serves. For more information, visit veeva.com.

³Ô¹Ï±¬ÁÏ Forward-looking Statements
This release contains forward-looking statements regarding ³Ô¹Ï±¬ÁÏ¡¯s products and services and the expected results or benefits from use of our products and services. These statements are based on our current expectations. Actual results could differ materially from those provided in this release and we have no obligation to update such statements. There are numerous risks that have the potential to negatively impact our results, including the risks and uncertainties disclosed in our filing on Form 10-K for the period ended January 31, 2022, which you can find (a summary of risks which may impact our business can be found on pages 13 and 14), and in our subsequent SEC filings, which you can access at .

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Contact:

Deivis Mercado
³Ô¹Ï±¬ÁÏ Systems
925-226-8821
deivis.mercado@veeva.com