More Than 75 Emerging Biotechs Use Veeva Basics Across Clinical, Regulatory, and Quality

Rhea-AI Summary

Veeva Systems (NYSE: VEEV) announced that over 75 biotechnology companies are now using Veeva Basics, their pre-configured and pre-validated software solution for clinical, regulatory, and quality operations. The company has introduced two new applications: Veeva CTMS Basics for clinical trial management and Veeva Submissions Publishing Basics for regulatory submissions.

The rapid adoption indicates a market shift from basic tools to comprehensive solutions that can scale with company growth. Available in North America and Europe, these solutions enable biotechs to deploy industry-leading software within weeks. Built on the Vault Platform, Veeva Basics allows customers to maintain current features and adapt their technology infrastructure as they expand.

Positive

• Over 75 biotech companies have adopted Veeva Basics, showing strong market penetration
• Expansion of product portfolio with two new applications (CTMS Basics and Submissions Publishing Basics)
• Geographic presence in both North America and Europe markets
• Platform designed for scalability, allowing companies to grow without changing systems

Negative

• None.

Delivers pre-configured, pre-validated software that can scale with the needs of fast-growing companies

PLEASANTON, Calif., May 20, 2025 /PRNewswire/ -- Veeva Systems (NYSE: VEEV) today announced that Veeva Basics is being used by more than 75 biotechs to gain efficiency and reduce costs across clinical, regulatory, and quality. With standardized applications, biotechs are going live with industry-leading software in weeks and gaining a system that can scale as they expand their business. The rapid adoption of Veeva Basics signals a shift from disparate entry-level tools toward complete, best-of-breed solutions that can support biotechs today and as they grow.

Designed specifically for fast-growing companies, Veeva Basics provides pre-configured and pre-validated solutions. This enables fast deployment and adoption regardless of company size. With clinical, regulatory, and quality solutions available, Veeva is adding two new applications for biotechs:

• Veeva CTMS Basics for clinical trial management, including milestones, monitoring, enrollment, issue resolution, and site communications.
• Veeva Submissions Publishing Basics for building, publishing, and transmitting regulatory submissions in a single system.

"More biotechs are adopting Veeva Basics in North America and Europe, driving savings in time, cost, and effort," said Steve Harper, general manager of Veeva Basics. "Our approach to deliver pre-configured and pre-validated solutions that can go live quickly is gaining momentum, and we're adding new clinical and regulatory solutions to meet the needs of high-growth companies. With complete cloud applications, biotechs can ensure they are always current and benefit from the latest features."

Veeva CTMS Basics and Submissions Publishing Basics are available today in North America and Europe. Built on the proven Vault Platform, Veeva Basics applications allow customers to scale their technology infrastructure as they grow. For more on Veeva Basics, visit veeva.com/VeevaBasics.

What biotechs are saying about Veeva Basics:
"I believe Veeva Basics is a game changer, giving smaller biotech companies access to the same modern and connected applications that are typically only available to larger organizations," said Ian Hodgson, Ph.D., chief operating officer at Corbus Pharmaceuticals, Inc. "As our company continues to grow, I am confident that Veeva's platform can scale with us and help ensure we remain up to date as regulatory requirements evolve."

"As we expand our studies to a larger scale, Veeva eTMF Basics gives us more control of our data and process to ensure inspection readiness," said Joe Thornton, associate director, clinical operations at Scancell. "Having an industry-leading solution with pre-configured best practices as our foundation for trials will help drive speed and innovation as we continue to develop novel immunotherapies."

"The global support and training provided with Veeva Basics helps us gain maximum value from Veeva's industry solution," said Rebecca Deng, Ph.D., associate director, regulatory affairs and QA systems at Terns Pharmaceuticals. "With a simple path to go live and validation, Veeva Basics has delivered significant time and resource savings."

About Veeva Systems
Veeva is the global leader in cloud software for the life sciences industry. Committed to innovation, product excellence, and customer success, Veeva serves more than 1,000 customers, ranging from the world's largest biopharmaceutical companies to emerging biotechs. As a Public Benefit Corporation, Veeva is committed to balancing the interests of all stakeholders, including customers, employees, shareholders, and the industries it serves. For more information, visit veeva.com.

Veeva Forward-looking Statements
This release contains forward-looking statements regarding Veeva's products and services and the expected results or benefits from use of our products and services, including certain of our new solutions and applications that are still under development or not generally available. These statements are based on our current expectations. Actual results, availability, and any future events relating to these products and services 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 fiscal year ended January 31, 2025, which you can find here (a summary of risks which may impact our business can be found on pages 9 and 10), and in our subsequent SEC filings, which you can access at sec.gov.

Contact:

Deivis Mercado
Veeva Systems
925-226-8821
deivis.mercado@veeva.com

 

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SOURCE Veeva Systems

FAQ

What is Veeva Basics and how many companies are using it?

Veeva Basics is a pre-configured, pre-validated software solution for clinical, regulatory, and quality operations. Over 75 biotech companies are currently using the platform.

What are the new applications launched by Veeva Systems (VEEV)?

Veeva Systems launched two new applications: Veeva CTMS Basics for clinical trial management and Veeva Submissions Publishing Basics for regulatory submissions.

Where is Veeva Basics available and how quickly can it be deployed?

Veeva Basics is available in North America and Europe, and can be deployed within weeks due to its pre-configured and pre-validated nature.

How does Veeva Basics help growing biotech companies?

Veeva Basics helps growing biotech companies by providing scalable, pre-configured solutions that can be deployed quickly, reduce costs, and adapt to company growth while maintaining current features and regulatory compliance.